NOVEMBER 2020 - Frontline Medical Supply

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NOVEMBER 2020 - Frontline Medical Supply
PRODUCT
C ATA L O G U E
        NOVEMBER 2020
NOVEMBER 2020 - Frontline Medical Supply
I NEED PROVEN
EXPERIENCE.
FRONTLINE CROSSINGS™ IS THE
SUPPLIER OF 1 BILLION+ UNITS OF
PPE TO PROVINCIAL MINISTRIES IN
CANADA.

I NEED A RUSH ORDER.
UP TO 200 MILLION NITRILE
GLOVES WITHIN 30 DAYS. DELIVERED.

I NEED QUALITY
ASSURANCE.
INDUSTRY LEADING NET
PAYMENT TERMS. QUALITY FIRST.
PAYMENT LATER.
NOVEMBER 2020 - Frontline Medical Supply
Welcome to Frontline Crossings™ Medical Supply.
 With headquarters in Vancouver, British Columbia, Frontline Crossings™ is a Health Canada
(MDEL #12101) and FDA (#3017375567) registered distributor of quality medical devices. As
       the supplier of over 1 billion units of PPE to Provincial Ministries across Canada,
Frontline Crossings™ supports large health care and government organizations by providing
   timely and secure access to a wide selection of professional-grade medical devices at
                                    wholesale discount pricing.

   FRONTLINE CROSSINGS™                                           of large-scale shipments of PPE is no small task.
   THE GOVERNMENT                                                 That is why more and more health care organiza-
   PROCUREMENT                                                    tions choose Frontline Crossings™ for its proven
   SPECIALISTS.                                                   ability to always get the job done. With offices in
                                                                  Vancouver (Canada) and Seattle (USA), Frontline
With a dedicated regulatory compliance team                       Crossings™ is able to leverage its global supply
supported by over 30 administrative staff,                        chain and logistics expertise to source and deliver
Frontline Crossings™ is ready to compete in any                   even the largest volumes of professional PPE
public sector tender process. Our references                      products.
from Canadian Provincial Ministries stand as a
testament to our ability to get the job done, on-
time, and with total customer satisfaction.
                                                                       IN STOCK. THE HIGHEST
                                                                       DEMAND PROFESSIONAL
                                                                       PRODUCTS FOR THE MOST
   SATISFACTION GUARANTEED.
                                                                       HIGH-RISK OPERATING
   NET PAYMENT TERMS FOR
                                                                       ENVIRONMENTS.
   QUALIFIED GOVERNMENT
   ORGANIZATIONS.                                                 In order to meet the strict quality demands of
                                                                  government health care organizations, Frontline
At Frontline Crossings™ we appreciate that
                                                                  Crossings™ offers access to a wide range of
building trust is the most important first step in
                                                                  professional PPE products. Frontline Crossings™
serving our government organizations and com-
                                                                  is the only Medical Device Establishment License
munity health care agencies. That is why Front-
                                                                  # in Canada registered to import the NIOSH
line Crossings™ offers qualified government cli-
                                                                  Surgical N95 (FDA) Particulate Respirator Model
ents net payment options, ensuring that quality
                                                                  DTC3M-1, a NIOSH-approved medical device
and customer satisfaction is guaranteed before
                                                                  with the highly sought-after FDA “surgical N95”
any payment is made. For government organiza-
                                                                  classification. Frontline Crossings™ is also a
tions outside of Canada, Frontline Crossings™ is
                                                                  high-volume purchaser of nitrile patient exam
proud to work with the support of Export Devel-
                                                                  gloves (up to 200 million gloves per month) from
opment Canada to help facilitate the delivery of
                                                                  Shandong Intco Medical Products Corporation,
needed PPE to government organizations abroad.
                                                                  one of the largest and most respected medical
                                                                  and surgical glove manufacturers in Asia. Because
                                                                  of the high volume of purchases and excellent
   EXPERIENCE MATTERS.                                            reputation worldwide, when it comes to large
   SUPPLIER OF OVER 1 BILLION+                                    institutional orders of professional PPE, Frontline
   UNITS OF PPE TO PROVINCIAL                                     Crossings™ offers some of the fastest delivery
   MINISTRIES IN CANADA.                                          times in the industry.
In an increasingly complex logistics and regu-
latory environment, ensuring on-time delivery
                                                        F R O N T L I N E C R O S S I N G S ™ M E D I C A L S U P P LY LT D .   3
                                   thefrontlinemedicalsupply.com | info@thefrontlinemedicalsupply.com | +1 604-558-5195
NOVEMBER 2020 - Frontline Medical Supply
List of Products
                                            N95 PARTICULATE RESPIRATORS

                                            NIOSH + Surgical N95 (FDA) Classification
                                            Dasheng NIOSH Surgical N95 - Model DTC3M-1................. 9
                                            Dasheng NIOSH Surgical N95 - Model DTC3B...................11

                                            NEW! Makrite NIOSH N95 Particulate Respirator.............. 13

                                            MEDICAL-GRADE PROTECTIVE FACE MASKS
                                            Adults
                                            NEW! Disposable Surgical Face Mask (Level 3)................. 15
    FA C E M A S K S &                      NEW! Disposable Surgical Face Mask - Tie-On (Level 3)... 17
    R E S P I R AT O R S
                                            NEW! Medical Face Mask + Built-In Protective Shield
                                            (Level 3).......................................................................... 19
                                            NEW! Custom Printed Disposable Face Mask (Level 1)..... 21

                                            Children
                                            Disposable Medical Face Mask (Level 1)........................... 23
                                            NEW! Custom Printed Disposable Face Mask (Level 1)..... 25

                                            NON-MEDICAL PROTECTIVE FACE MASKS
                                            Adults
                                            Disposable 3-Ply Protective Face Mask............................ 27

                                          ORDER FORMS ON PAGE 77

4          F R O N T L I N E C R O S S I N G S ™ M E D I C A L S U P P LY LT D .
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NOVEMBER 2020 - Frontline Medical Supply
NITRILE GLOVES
                                         Nitrile Exam Gloves - MDALL Listed (Powder Free)........... 31
                                         NEW! Nitrile Exam Gloves - 9” Cuff (Powder Free)............ 33
    PROTECTIVE
      G L OV E S                         NEW! Nitrile Exam Gloves - 12” Cuff (Powder Free).......... 35

                                         VINYL GLOVES
                                         Vinyl Exam Gloves (Powder Free)..................................... 37

                                         FACE SHIELDS
                                         Medical Isolation Face Shield with Head Strap.................. 41
       EYE
    PROTECTION
                                         GOGGLES
                                         Medical Protective Goggles with Head Strap.................... 43

                                         NON-SURGICAL ISOLATION GOWNS
                                         Non-Surgical Isolation Gown ANSI/AAMI
                                         PB70:2012 (Level 3)......................................................... 47
                                         Non-Surgical Isolation Gown ANSI/AAMI
    PROTECTIVE                           PB70:2012 (Level 1)......................................................... 49
     CLOTHING
                                         Non-Surgical Isolation Gown ANSI/AAMI
                                         PB70:2012 (Level 2)......................................................... 51

                                         PROTECTIVE COVERALLS
                                         Medical Protective Clothing (EN14605 Type 4)................. 53

                                       ORDER FORMS ON PAGE 77

5       F R O N T L I N E C R O S S I N G S ™ M E D I C A L S U P P LY LT D .
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NOVEMBER 2020 - Frontline Medical Supply
HEAD COVERS
    PROTECTIVE                             Bouffant Head Cover....................................................... 57
     CLOTHING
    AC C E S S O R I E S                   SHOE COVERS
                                           Medical Isolation Shoe Cover........................................... 59

                                           INFRARED
T HE R M OM E T ERS
                                           Infrared Forehead Thermometer..................................... 63

                                           SYRINGES & NEEDLES
                                           Safety Hypodermic Needle – 25G x 1”.............................. 67

     SYRINGES &                            Safety Hypodermic Needle – 25G x 1.5”........................... 69
      NEEDLES                              Blunt Fill Safety Hypodermic Needle – 18G x 1”................ 71
                                           Blunt Fill Safety Hypodermic Needle – 18G x 1.5”............. 73
                                           Luer Lock Syringe............................................................ 75

                                         ORDER FORMS ON PAGE 77

6         F R O N T L I N E C R O S S I N G S ™ M E D I C A L S U P P LY LT D .
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NOVEMBER 2020 - Frontline Medical Supply
7   F R O N T L I N E C R O S S I N G S ™ M E D I C A L S U P P LY LT D .
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NOVEMBER 2020 - Frontline Medical Supply
Respirators &
                                    Face Masks
8   F R O N T L I N E C R O S S I N G S ™ M E D I C A L S U P P LY
                                                                F R LT
                                                                    O NDT. L I N E C R O S S I N G S ™ M E D I C A L S U P P LY LT D .   8
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                                    thefrontlinemedicalsupply.com
                                                         | +1 604-558-5195
                                                                  | info@thefrontlinemedicalsupply.com | +1 604-558-5195
NOVEMBER 2020 - Frontline Medical Supply
FL-M001

NIOSH SURGICAL
N95 (FDA) PARTICULATE
RESPIRATOR
DASHENG MODEL DTC3M-1
NOVEMBER 2020 - Frontline Medical Supply
PRODUCT DESCRIPTION                                                                 PAC K AG I N G I N F O R M AT I O N

■ NIOSH Surgical N95 (FDA) Particulate                                              ■ 20 respirators per box (box dimensions:
  Respirator designed to achieve a very close                                         14.5cm x 13.5cm x 16cm)
  facial fit and very efficient filtration of airborne                              ■ 400 respirators per carton (carton dimensions:
  particles (filtering out at least 95% of airborne                                   69.5cm x 31cm x 34cm)
  particles including large and small particles)
■ Registered with the National Institute for
  Occupational Safety and Health (NIOSH)                                            N A M E O F M A N U FAC T U R E R
  under Approval Number: TC-84A-4331                                                ■ Shanghai Dasheng Health Products
■ White colour                                                                         Manufacture Co., Ltd.
■ For single use only

                                                                                    M A N U FAC T U R E R A D D R E S S
M AT E R I A L / D I M E N S I O N S                                                ■ No. 228 Shihui Road, Songjiang, Shanghai,
■ Large size round “cup” design                                                        China 201613
■ 3-layer, PP nonwoven with meltblown filtration
  layer
■ Double headband strap
■ 15.5cm x 13.5cm                                                                      What is a Surgical N95?
                                                                                        A surgical N95 respirator is a NIOSH-approved
                                                                                        N95 respirator that has also been cleared by
                                                                                        the Food and Drug Administration (FDA) as
F E AT U R E S
                                                                                        a surgical mask. To verify the FDA clearance
■ Aluminum “arc” nose clip to offer a better fit                                        please contact the FDA at 1-800-638-2041.

■ Effective against particulate aerosols free of oil                                   What is NIOSH?
                                                                                        The National Institute for Occupational Safety
                                                                                        and Health (NIOSH) is the division of The
Q U A L I T Y S TA N DA R D &                                                           Centers for Disease Control and Prevention
                                                                                        (CDC) responsible for conducting research
T E S T I N G C E R T I F I C AT I O N S                                                and making recommendations for the pre-
■ NIOSH Approval Number TC-84A-4331                                                     vention of work-related injury and illness. Al-
                                                                                        though NIOSH is generally characterized as a
■ Surgical N95 designation (FDA)                                                        non-regulatory agency, guidance and recom-
■ CE                                                                                    mendations issued by NIOSH are often used
                                                                                        by other agencies responsible for developing
■ The respirator cup is labelled with the following                                     and enforcing workplace safety and health
     information as required by Federal Government                                      regulations.
     of Canada guidelines:
                                                                                       What is CE?
     • Manufacturer’s name                                                              CE marking is a certification mark that
     • NIOSH approval number                                                            indicates conformity with health, safety,
     • LOT number                                                                       and environmental protection standards for
                                                                                        products sold within the European Economic
     • Filter designation                                                               Area (EEA). The CE marking is also found on
                                                                                        products sold outside the EEA that have been
                                                                                        manufactured to EEA standards.
E X P I R AT I O N DAT E

■ 3 years from production date (as indicated on
     product packaging)

10          F R O N T L I N E C R O S S I N G S ™ M E D I C A L S U P P LY LT D .
            Frontlinecrossings.com | info@frontlinecrossings.com | +1 604-558-5195
FL-M002

NIOSH SURGICAL
N95 (FDA) PARTICULATE
RESPIRATOR
DASHENG MODEL DTC3B
PRODUCT DESCRIPTION                                                                 PAC K AG I N G I N F O R M AT I O N

■ NIOSH Surgical N95 (FDA) Particulate                                              ■ 20 respirators per box (box dimensions:
  Respirator designed to achieve a very close                                         14.5cm x 13.5cm x 16cm)
  facial fit and very efficient filtration of airborne                              ■ 400 respirators per carton (carton dimensions:
  particles (filtering out at least 95% of airborne                                   69.5cm x 31cm x 34cm)
  particles including large and small particles)
■ Registered with the National Institute for
                                                                                    N A M E O F M A N U FAC T U R E R
  Occupational Safety and Health (NIOSH)
  under Approval Number: TC-84A-4336                                                ■ Shanghai Dasheng Health Products
■ White colour                                                                         Manufacture Co., Ltd.
■ For single use only

                                                                                    M A N U FAC T U R E R A D D R E S S
M AT E R I A L / D I M E N S I O N S                                                ■ No. 228 Shihui Road, Songjiang, Shanghai,
■ Fold-flat horizontal “cone” design                                                   China 201613
■ 3-layer, PP nonwoven with meltblown
  filtration layer
■ Double headband strap
■ 17.5cm x 9.5cm                                                                       What is a Surgical N95?
                                                                                        A surgical N95 respirator is a NIOSH-approved
                                                                                        N95 respirator that has also been cleared by
                                                                                        the Food and Drug Administration (FDA) as
F E AT U R E S
                                                                                        a surgical mask. To verify the FDA clearance
■ Aluminum “arc” nose clip to offer a better fit                                        please contact the FDA at 1-800-638-2041.

■ Effective against particulate aerosols free of oil                                   What is NIOSH?
                                                                                        The National Institute for Occupational Safety
                                                                                        and Health (NIOSH) is the division of The
Q U A L I T Y S TA N DA R D &                                                           Centers for Disease Control and Prevention
                                                                                        (CDC) responsible for conducting research
T E S T I N G C E R T I F I C AT I O N S                                                and making recommendations for the pre-
■ NIOSH Approval Number TC-84A-4336                                                     vention of work-related injury and illness. Al-
                                                                                        though NIOSH is generally characterized as a
■ Surgical N95 designation (FDA)                                                        non-regulatory agency, guidance and recom-
■ CE                                                                                    mendations issued by NIOSH are often used
                                                                                        by other agencies responsible for developing
■ The respirator cup is labelled with the following                                     and enforcing workplace safety and health
     information as required by Federal Government                                      regulations.
     of Canada guidelines:
                                                                                       What is CE?
     • Manufacturer’s name                                                              CE marking is a certification mark that
     • NIOSH approval number                                                            indicates conformity with health, safety,
     • LOT number                                                                       and environmental protection standards for
                                                                                        products sold within the European Economic
     • Filter designation                                                               Area (EEA). The CE marking is also found on
                                                                                        products sold outside the EEA that have been
                                                                                        manufactured to EEA standards.
E X P I R AT I O N DAT E

■ 3 years from production date (as indicated on
     product packaging)

12          F R O N T L I N E C R O S S I N G S ™ M E D I C A L S U P P LY LT D .
            Frontlinecrossings.com | info@frontlinecrossings.com | +1 604-558-5195
FL-M003

MAKRITE™ NIOSH N95
PARTICULATE
RESPIRATOR
MODEL 9500-N95 (ADULT)
PRODUCT DESCRIPTION                                                                 E X P I R AT I O N DAT E

■ NIOSH N95 particulate respirator designed to                                      ■ 3 years from production date (as indicated on
  achieve a very close facial fit and very efficient                                   product packaging)
  filtration of airborne particles (filtering out at
  least 95% of airborne particles including large
                                                                                    PAC K AG I N G I N F O R M AT I O N
  and small particles)
                                                                                    ■ 20 respirators per box (box dimensions: 14cm x
■ Registered with the National Institute for
  Occupational Safety and Health (NIOSH)                                               20cm x 13cm)
  under Approval Number: TC-84A-5411
■ White colour                                                                      N A M E O F M A N U FAC T U R E R
■ For single use only
                                                                                    ■ Dongguan Sure_On Plastic & Fiber Products
                                                                                       Co., Ltd.
M AT E R I A L / D I M E N S I O N S

■ Round “cup” design                                                                M A N U FAC T U R E R A D D R E S S
■ 3-layer, PP nonwoven with meltblown filtration                                    ■ ZhuFo Ling Industrial Area, TangXia Town,
  layer                                                                                DongGuan City, GuangDong, China
■ Double headband strap
■ 14cm x 12cm

F E AT U R E S
                                                                                       What is NIOSH?
■ Aluminum “arc” nose clip to offer a better fit                                        The National Institute for Occupational Safety
                                                                                        and Health (NIOSH) is the division of The
■ Effective against particulate aerosols free of oil
                                                                                        Centers for Disease Control and Prevention
                                                                                        (CDC) responsible for conducting research
                                                                                        and making recommendations for the pre-
Q U A L I T Y S TA N DA R D &                                                           vention of work-related injury and illness. Al-
                                                                                        though NIOSH is generally characterized as a
T E S T I N G C E R T I F I C AT I O N S
                                                                                        non-regulatory agency, guidance and recom-
■ NIOSH Approval Number TC-84A-5411                                                     mendations issued by NIOSH are often used
                                                                                        by other agencies responsible for developing
■ CE                                                                                    and enforcing workplace safety and health
■ The respirator cup is labelled with the following                                     regulations.
     information:
                                                                                       What is CE?
     • Manufacturer’s name                                                              CE marking is a certification mark that
     • NIOSH approval number                                                            indicates conformity with health, safety,
                                                                                        and environmental protection standards for
     • Filter designation
                                                                                        products sold within the European Economic
                                                                                        Area (EEA). The CE marking is also found on
                                                                                        products sold outside the EEA that have been
                                                                                        manufactured to EEA standards.

14          F R O N T L I N E C R O S S I N G S ™ M E D I C A L S U P P LY LT D .
            Frontlinecrossings.com | info@frontlinecrossings.com | +1 604-558-5195
FL-M073

DISPOSABLE SURGICAL
FACE MASK (LEVEL 3)
MODEL USL301A (ADULT)
PRODUCT DESCRIPTION                                                                 E X P I R AT I O N DAT E

■ Disposable surgical mask with ear loop and                                        ■ 2 years from production date (as indicated on
     adjustable nose bar                                                               product packaging)
■    ASTM F2100 Level 3
■    Non-sterile                                                                    PAC K AG I N G I N F O R M AT I O N
■    Blue colour                                                                    ■ 50 face masks in 1 sealed polybag (package
■    For single use only                                                              dimensions: 19.5cm x 10.5cm x 8.5cm)
                                                                                    ■ 40 face masks per box (box dimensions:
M AT E R I A L / D I M E N S I O N S                                                  53.5cm x 40cm x 36cm)

■ 3-layer mask: 2 layer non-woven and
  1 middle-layer meltblown filtration material                                      N A M E O F M A N U FAC T U R E R
■ Ear-loop strap                                                                    ■ The Aleen International Corporation
■ 17.5cm x 9.5cm

                                                                                    M A N U FAC T U R E R A D D R E S S
F E AT U R E S
                                                                                    ■ Jiutian Green Science And Technology Industri-
■ Adaptable/adjustable nose bar                                                        al Park, Heyuan High-tech Zone, Heyuan,
■ Multi-layer filtration                                                               Guangdong, 517000, China

Q U A L I T Y S TA N DA R D &
                                                                                       What is CE?
T E S T I N G C E R T I F I C AT I O N S                                                CE marking is a certification mark that
                                                                                        indicates conformity with health, safety,
■ ASTM F2100 LEVEL 3:
                                                                                        and environmental protection standards for
     • Bacterial filtration efficiency                                                  products sold within the European Economic
       (ASTM F2101): ≥99%                                                               Area (EEA). The CE marking is also found on
                                                                                        products sold outside the EEA that have been
     • Differential pressure performance level                                          manufactured to EEA standards.
       (EN 14683:2019):
FL-M074

DISPOSABLE SURGICAL
FACE MASK - TIE-ON
(LEVEL 3)
MODEL USL301A-S (ADULT)
PRODUCT DESCRIPTION                                                                 E X P I R AT I O N DAT E

■ Disposable surgical mask with tie-on straps                                       ■ 2 years from production date (as indicated on
     and adjustable nose bar                                                           product packaging)
■    ASTM F2100 Level 3
■    Non-sterile                                                                    PAC K AG I N G I N F O R M AT I O N
■    Blue colour                                                                    ■ 50 face masks in 1 sealed polybag (package
■    For single use only                                                              dimensions: 19.5cm x 10.5cm x 13cm)
                                                                                    ■ 40 face masks per box (box dimensions:
M AT E R I A L / D I M E N S I O N S                                                  54.5cm x 40.5cm x 54cm)

■ 3-layer mask: 2 layer non-woven and
  1 middle-layer meltblown filtration material                                      N A M E O F M A N U FAC T U R E R
■ Tie-on horizontal straps                                                          ■ The Aleen International Corporation
■ 17.5cm x 9.5cm

                                                                                    M A N U FAC T U R E R A D D R E S S
F E AT U R E S
                                                                                    ■ Jiutian Green Science And Technology Industri-
■ Adaptable/adjustable nose bar                                                        al Park, Heyuan High-tech Zone, Heyuan,
■ Multi-layer filtration                                                               Guangdong, 517000, China

Q U A L I T Y S TA N DA R D &
                                                                                       What is CE?
T E S T I N G C E R T I F I C AT I O N S                                                CE marking is a certification mark that
                                                                                        indicates conformity with health, safety,
■ ASTM F2100 LEVEL 3:
                                                                                        and environmental protection standards for
     • Bacterial filtration efficiency                                                  products sold within the European Economic
       (ASTM F2101): ≥99%                                                               Area (EEA). The CE marking is also found on
                                                                                        products sold outside the EEA that have been
     • Differential pressure performance level                                          manufactured to EEA standards.
       (EN 14683:2019):
FL-M075

NEW! EXCLUSIVE INNOVATION

MEDICAL FACE MASK +
BUILT-IN PROTECTIVE
SHIELD (LEVEL 3)
MODEL USL301-V (ADULT)
PRODUCT DESCRIPTION                                                                 E X P I R AT I O N DAT E

■ EXCLUSIVE TECHNOLOGY FROM                                                         ■ 2 years from production date (as indicated on
     FRONTLINE CROSSINGS™                                                              product packaging)
■    2 in 1 surgical face mask plus protective shield
     combination                                                                    PAC K AG I N G I N F O R M AT I O N
■    ASTM F2100 Level 3
                                                                                    ■ 10 face masks with shields in 1 sealed polybag
■    Medical grade & disposable                                                       (package dimensions: 23cm x 35cm x18cm)
■    Non-sterile                                                                    ■ 40 face masks with shields per box (box di-
■    Blue colour                                                                      mensions: 55cm x 47.5cm x 37.5cm)
■    For single-use only

                                                                                    N A M E O F M A N U FAC T U R E R
M AT E R I A L / D I M E N S I O N S
                                                                                    ■ The Aleen International Corporation
■ 3-layer mask: 2 layers non-woven and 1
  middle-layer meltblown filtration material
■ Ear-loop straps                                                                   M A N U FAC T U R E R A D D R E S S
■ 17.5cm x 9.5cm (face mask) / 			                                                  ■ Jiutian Green Science And Technology Industri-
  220cm x 120cm (shield)                                                               al Park, Heyuan High-tech Zone, Heyuan,
                                                                                       Guangdong, 517000, China
F E AT U R E S

■ Adaptable nose bar
                                                                                       What is CE?
■ Multi-layer filtration protection                                                     CE marking is a certification mark that
                                                                                        indicates conformity with health, safety,
■ Built-in removable protective shield 		                                               and environmental protection standards for
     attachment                                                                         products sold within the European Economic
                                                                                        Area (EEA). The CE marking is also found on
                                                                                        products sold outside the EEA that have been
                                                                                        manufactured to EEA standards.
Q U A L I T Y S TA N DA R D &
T E S T I N G C E R T I F I C AT I O N S                                               What is ASTM F2100?
                                                                                        ASTM F2100 is a standardized testing spec-
■ ASTM F2100 LEVEL 3:                                                                   ification that classifies medical face mask
     • Bacterial filtration efficiency                                                  material performance. Medical face mask
       (ASTM F2101): ≥99%                                                               materials are designated as one or more of
                                                                                        the following performance classes: Level 1
     • Differential pressure performance level                                          barrier, Level 2 barrier, and Level 3 barrier.
       (EN 14683:2019):
FL-M012

CUSTOM PRINTED
DISPOSABLE FACE
MASKS (LEVEL 1)
MODEL: USL 103A (ADULT)
PRODUCT DESCRIPTION                                                                 E X P I R AT I O N DAT E

■ EXCLUSIVE TECHNOLOGY FROM                                                         ■ 2 years from production date (as indicated on
     FRONTLINE CROSSINGS™                                                              product packaging)
■    Disposable medical face mask
■    ASTM F2100 Level 1                                                             PAC K AG I N G I N F O R M AT I O N
■    Novel printing technology allows for custom                                    ■ 50 face masks sealed in 1 polybag (package
     graphic designs and colour combinations                                          dimensions: 19.5cm x 10.5cm x 8.5cm)
■    Non-sterile                                                                    ■ 50 face masks per 1 box (box dimensions:
■    For single-use only                                                              53.5cm x 40cm x 36cm)

M AT E R I A L / D I M E N S I O N S
                                                                                    N A M E O F M A N U FAC T U R E R
■ 3-layer mask: 2 layer non-woven and 1
                                                                                    ■ The Aleen International Corporation
  middle-layer meltblown polypropylene
■ Ear-loop strap
■ 17.5cm x 9.5cm                                                                    M A N U FAC T U R E R A D D R E S S

                                                                                    ■ Jiutian Green Science And Technology Industri-
                                                                                       al Park, Heyuan High-tech Zone, Heyuan,
F E AT U R E S
                                                                                       Guangdong, 517000, China
■ Novel printing technology allows for custom
     graphic designs and colour combinations
■ Breathable with adjustable nose clip                                                 What is CE?
■ 3-ply layer filtration protection                                                     CE marking is a certification mark that
                                                                                        indicates conformity with health, safety,
                                                                                        and environmental protection standards for
                                                                                        products sold within the European Economic
Q U A L I T Y S TA N DA R D &                                                           Area (EEA). The CE marking is also found on
T E S T I N G C E R T I F I C AT I O N S                                                products sold outside the EEA that have been
                                                                                        manufactured to EEA standards.
■ ASTM F2100 (Level 1):
                                                                                       What is ASTM F2100?
     • Bacterial filtration efficiency
                                                                                        ASTM F2100 is a standardized testing spec-
       (ASTM F2101): ≥95%                                                               ification that classifies medical face mask
                                                                                        material performance. Medical face mask
     • Differential pressure performance level
                                                                                        materials are designated as one or more of
       (EN 14683:2019):
FL-M008

DISPOSABLE
MEDICAL FACE MASK
(TYPE 1)
MODEL: FL-M011 (CHILD)
PRODUCT DESCRIPTION                                                                   E X P I R AT I O N DAT E

■ Smaller mask dimensions designed to ensure a                                        ■ 2 years from production date (as indicated on
     better protective fit for younger users               5
                                                                                         product packaging)
■    ASTM F2100 Level 1
■    Non-sterile                                                                      PAC K AG I N G I N F O R M AT I O N
■    Blue/white colour                                                                ■ 10 face masks sealed in 1 polybag (package
■    For single use only                                                                dimensions 19cm x 11cm)
                                                                                      ■ 50 face masks per 1 box (box dimensions:
M AT E R I A L / D I M E N S I O N S                                                    16cm x 8cm x 9.5cm)
■ 3-layer: 2 layer non-woven and 1 middle-layer
  meltblown polypropylene
                                                                                      N A M E O F M A N U FAC T U R E R
■ Ear-loop strap
                                                                                      ■ Hunan EEXI Technology & Service Co., Ltd.
■ Smaller mask dimensions: 14.5cm x 9.0cm

F E AT U R E S                                                                        M A N U FAC T U R E R A D D R E S S

■ Breathable with adjustable nose clip                                                ■ No. 6, North of Pingtou Road, Liuyang Hi-tech
■ 3-ply layer filter structure protection                                                Industrial development zone, Hunan Province,
                                                                                         China

Q U A L I T Y S TA N DA R D &
T E S T I N G C E R T I F I C AT I O N S                                                 What is CE?
                                                                                          CE marking is a certification mark that
■ ASTM F2100 (Level 1)                                                                    indicates conformity with health, safety,
     • Bacterial filtration efficiency                                                    and environmental protection standards for
       (ASTM F2101): ≥95%                                                                 products sold within the European Economic
                                                                                          Area (EEA). The CE marking is also found on
     • Differential pressure performance level                                            products sold outside the EEA that have been
       (EN 14683:2019):
FL-M011

CUSTOM PRINTED
DISPOSABLE FACE
(LEVEL 1)
MODEL: CN000502C (CHILD)
PRODUCT DESCRIPTION                                                                   E X P I R AT I O N DAT E

■ Disposable medical face mask                                                        ■ 2 years from production date (as indicated on
■ ASTM F2100 Level 1                                                                     product packaging)
■ Smaller mask dimensions for a better
  protective fit for younger users5                                                   PAC K AG I N G I N F O R M AT I O N
■ Novel printing technology allows for custom                                         ■ 25 or 50 face masks sealed in 1 polybag
  graphic designs                                                                       (polybag dimensions 19.5cm x 10.5cm x8.5cm
■ Non-sterile                                                                           or 19.5cm X 10.5cm X 4.25cm)
■ For single-use only                                                                 ■ 25 or 50 face masks per 1 box (box dimensions:
                                                                                        53.5cm x 40cm x 36cm)
M AT E R I A L / D I M E N S I O N S

■ 3-layer: 2 layer non-woven and 1 middle-layer                                       N A M E O F M A N U FAC T U R E R
  meltblown polypropylene
                                                                                      ■ The Aleen International Corporation
■ Ear-loop strap
■ Smaller mask dimensions: 14.5cm x 9.0cm
                                                                                      M A N U FAC T U R E R A D D R E S S

F E AT U R E S                                                                        ■ Jiutian Green Science And Technology Indus-
                                                                                         trial Park, Heyuan High-tech Zone, Heyuan,
■ Novel printing technology allows for custom
                                                                                         Guangdong, 517000, China
  graphic designs
■ Breathable with adjustable nose clip
■ 3-ply layer filtration protection                                                      What is CE?
                                                                                          CE marking is a certification mark that
                                                                                          indicates conformity with health, safety,
Q U A L I T Y S TA N DA R D &                                                             and environmental protection standards for
T E S T I N G C E R T I F I C AT I O N S                                                  products sold within the European Economic
                                                                                          Area (EEA). The CE marking is also found on
■ ASTM F2100 (Level 1)                                                                    products sold outside the EEA that have been
                                                                                          manufactured to EEA standards.
     • Bacterial filtration efficiency
       (ASTM F2101): ≥95%                                                                What is ASTM F2100?
     • Differential pressure performance level                                            ASTM F2100 is a standardized testing spec-
                                                                                          ification that classifies medical face mask
       (EN 14683:2019):
FL-M010

DISPOSABLE 3-PLY
PROTECTIVE FACE MASK
(NON-MEDICAL)
PRODUCT DESCRIPTION                                                                 E X P I R AT I O N DAT E

■ Our most affordable disposable 3-ply face                                         ■ 5 years from production date
  mask for daily use
■ Non-medical grade                                                                 PAC K AG I N G I N F O R M AT I O N
■ White colour
                                                                                    ■ 50 face masks per box (box dimensions:
■ For single use only                                                                  57cm x 41.5cm x 40cm)

M AT E R I A L / D I M E N S I O N S
                                                                                    N A M E O F M A N U FAC T U R E R
■ 2 layer non-woven and 1 middle-layer melt-
                                                                                    ■ Jiangsu Bailian Medical Technology Co., Ltd.
  blown filtration material with adaptable nose
  bar
■ Ear-loop strap                                                                    M A N U FAC T U R E R A D D R E S S
■ 17.5cm x 9.5cm                                                                    ■ 9th Floor, Block G116, Hi-Tech Medical Indus-
                                                                                       trial Park, Taizhou, Jiangsu, China
F E AT U R E S

■ Ultra-soft non-woven material
■ Non-medical grade
■ 3-ply layer filter structure protection

Q U A L I T Y S TA N DA R D &
T E S T I N G C E R T I F I C AT I O N S

■ Non-medical grade

28          F R O N T L I N E C R O S S I N G S ™ M E D I C A L S U P P LY LT D .
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GLOVE SIZING CHART

        Sizes                         XS                        S                        M                         L                          XL

Length (mm)                     235±5mm                  235±5mm                  235±5mm                   235±5mm                  235±5mm

Palm Width                       75±5mm                   85±5mm                   95±5mm                   110±5mm                  120±5mm

Thumb L.                         52±2mm                   54±2mm                   57±2mm                   59±2mm                    65±2mm

Forefinger L.                    66±2mm                   68±2mm                   72±2mm                   74±2mm                   80±2mm

Middle finger L.                 77±2mm                   79±2mm                   82±2mm                   85±2mm                    92±2mm

Ring finger L.                   68±2mm                   71±2mm                   75±2mm                   77±2mm                   82±2mm

Little finger L.                 52±2mm                   54±2mm                   56±2mm                   60±2mm                   64±2mm

                                                                Protective
                                                                   Gloves
30       F R O N T L I N E C R O S S I N G S ™ M E D I C A L S U P P LY
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                                                                         O NDT. L I N E C R O S S I N G S ™ M E D I C A L S U P P LY LT D .        30
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FL-GLV1

NITRILE EXAM GLOVES
MDALL LISTED
(POWDER FREE )

                      Actual packaging may vary by market.
PRODUCT DESCRIPTION                                                                 N A M E O F M A N U FAC T U R E R
■ Disposable nitrile gloves for patient examina-                                    ■ Shandong Intco Medical Products Co., Ltd.
  tion
■ 100% latex-free                                                                   M A N U FAC T U R E R A D D R E S S
■ Blue colour
                                                                                    ■ Qiwang Road, Naoshan Industrial Park,
■ For single use only
                                                                                       Qingzhou, Weifang, Shandong, China 262500
M AT E R I A L / D I M E N S I O N S
■ 100% nitrile rubber (acrylonitrile butadiene)                                        What is CE?
■ 100% latex free                                                                       CE marking is a certification mark that
■ Cuff length: 9” (230mm)                                                               indicates conformity with health, safety,
                                                                                        and environmental protection standards for
■ Powder free                                                                           products sold within the European Economic
■ Available in 4 sizes:                                                                 Area (EEA). The CE marking is also found on
                                                                                        products sold outside the EEA that have been
     • Small, Medium, Large, X-Large
                                                                                        manufactured to EEA standards.

F E AT U R E S
                                                                                       What is ASTM D6319-10?
■ Ambidextrous                                                                          ASTM D6319 is a standardized laboratory
■ Excellent bacteriophage penetration resistance7                                       testing method that evaluates requirements
                                                                                        for nitrile rubber gloves used in conducting
■ High tensile properties and puncture resistance                                       medical examinations and diagnostic and
                                                                                        therapeutic procedures.
Q U A L I T Y S TA N DA R D &
T E S T I N G C E R T I F I C AT I O N S                                               What is ASTM F1671-2013?
                                                                                        ASTM F1671 is a standardized laboratory
■ ASTM D6319-10                                                                         testing method that evaluates resistance
■ ASTM F1671-2013                                                                       of materials used in protective clothing to
■ EN 374-4:2013: Resistance to degradation of                                           penetration by blood-borne pathogens using
                                                                                        phi-X174 bacteriophage penetration as a test
     chemicals
                                                                                        system.
■ EN 374-1:2003: Minimum liquid proof length
■ EN 374-2:2014: Determination of resistance                                           What is EN455-1,2,3,4?
     penetration                                                                        EN455 is a standardized testing method
                                                                                        developed by the European Committee for
■    EN 455-1:2000: Freedom from holes                                                  Standardization (CEN) to evaluate any glove
■    EN 455-2:2015: Force at break                                                      that could be used for medical work:
■    EN 455-3:2015: Aqueous extractable protein                                         • Part 1 refers to requirements and testing of
■    MDALL License Number: 93926                                                          gloves for freedom from holes
                                                                                        • Part 2 refers to requirements and tests for
■    CE                                                                                   physical properties
                                                                                        • Part 3 refers to requirements and tests for
E X P I R AT I O N DAT E                                                                  biological evaluation
■ 5 years from production date                                                          • Part 4 refers to requirements and testing
                                                                                          for shelf life determination
PAC K AG I N G I N F O R M AT I O N
                                                                                       What is MDALL?
■ 100 gloves per box (box dimensions: 23.0cm x                                          The Medical Devices Bureau (Bureau) of the
     12.5cm x 6cm)                                                                      Therapeutic Products Directorate, Health
                                                                                        Canada is the Canadian federal regulator
                                                                                        responsible for licensing medical devices in
                                                                                        accordance with the Food and Drugs Act and
                                                                                        Regulations and the Medical Devices Regu-
                                                                                        lations. The Bureau maintains a database of
                                                                                        all licensed Class II, III, and IV medical devices
                                                                                        offered for sale in Canada called the Medical
                                                                                        Devices Active Listing (MDALL)
6
  MDALL reference as VFORCE nitrile glove. Amended to the Synguard
trademark by way of Interim Order Application Number: 315622
7
  ASTM F1671-2013

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FL-GLV4

NITRILE EXAM GLOVES
9” CUFF
(POWDER FREE)

                 Actual packaging may vary by market.
PRODUCT DESCRIPTION                                                                 N A M E O F M A N U FAC T U R E R
■ Disposable nitrile gloves for patient                                             ■ Hebei Titans Hongsen Medical Technology Co.
  examination                                                                          Ltd.
■ Single use, disposable
                                                                                    M A N U FAC T U R E R A D D R E S S
M AT E R I A L / D I M E N S I O N S
■ 100% nitrile rubber (acrylonitrile butadiene)                                     ■ Eastern Industrial Zone, Nangong City, Xingtai
■ Cuff Length: 9” (230mm)                                                              City, Hebei China
■ Width: 75-115mm (depends on size)
■ Thickness: 0.06 - 0.09mm                                                             What is CE?
■ Weight: 3.5g                                                                          CE marking is a certification mark that
                                                                                        indicates conformity with health, safety,
■ Tensile Strength: 15-26 Mpa                                                           and environmental protection standards for
■ Stretch: 500-520%                                                                     products sold within the European Economic
                                                                                        Area (EEA). The CE marking is also found on
■ Available in 4 sizes:                                                                 products sold outside the EEA that have been
     • Small, Medium, Large, X-Large                                                    manufactured to EEA standards.

F E AT U R E S                                                                         What is EN455-1,2,3,4?
                                                                                        EN455 is a standardized testing method
■    Powder free
                                                                                        developed by the European Committee for
■    Strong and puncture resistant                                                      Standardization (CEN) to evaluate any glove
■    Bacteria/chemical/acid and alkali resistant                                        that could be used for medical work:
                                                                                        • Part 1 refers to requirements and testing of
■    Soft, comfortable and flexible
                                                                                          gloves for freedom from holes
■    High sensitivity                                                                   • Part 2 refers to requirements and tests for
■    Clean and anti-static                                                                physical properties
                                                                                        • Part 3 refers to requirements and tests for
■    Non-toxic
                                                                                          biological evaluation
■    Ambidextrous                                                                       • Part 4 refers to requirements and testing
                                                                                          for shelf life determination
Q U A L I T Y S TA N DA R D &
T E S T I N G C E R T I F I C AT I O N S
■    FDA 510(k) registered
■    Health Canada (Interim Order Authorization)
■    ISO 13485 & ISO 9001:2015
■    EN 455 & EN374
■    CE
E X P I R AT I O N DAT E
■ 5 years from date of manufacture

PAC K AG I N G I N F O R M AT I O N
■    100 gloves per box
■    10 boxes/1000 gloves per case
■    Box dimensions: 235 x 125 x 68mm
■    Case dimensions: 365 x 265 x 255mm

34          F R O N T L I N E C R O S S I N G S ™ M E D I C A L S U P P LY LT D .
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FL-GLV3

NITRILE CHEMO-RATED
GLOVES
12” CUFF
(POWDER FREE)

                      Actual packaging may vary by market.
PRODUCT DESCRIPTION                                                                 N A M E O F M A N U FAC T U R E R
■ Nitrile disposable chemo-rated gloves                                             ■ Hebei Titans Hongsen Medical Technology Co.
■ Single use, disposable                                                               Ltd.
M AT E R I A L / D I M E N S I O N S
                                                                                    M A N U FAC T U R E R A D D R E S S
■ 100% nitrile rubber (acrylonitrile butadiene)
■ Cuff Length: 12” (295mm)                                                          ■ Eastern Industrial Zone, Nangong City, Xingtai
■ Width: 75-115mm (depends on size)                                                    City, Hebei China
■ Thickness: 0.07 - 0.13mm
■ Weight: 6.0g                                                                         What is CE?
■ Tensile Strength: 31-41 Mpa                                                           CE marking is a certification mark that
                                                                                        indicates conformity with health, safety,
■ Stretch: 510-540%                                                                     and environmental protection standards for
■ Available in 4 sizes:                                                                 products sold within the European Economic
                                                                                        Area (EEA). The CE marking is also found on
     • Small, Medium, Large, X-Large                                                    products sold outside the EEA that have been
                                                                                        manufactured to EEA standards.
F E AT U R E S
■    Powder free                                                                       What is EN455-1,2,3,4?
                                                                                        EN455 is a standardized testing method
■    Chemo-drug rated                                                                   developed by the European Committee for
■    Strong and puncture resistant                                                      Standardization (CEN) to evaluate any glove
■    Bacteria/chemical/acid and alkali resistant                                        that could be used for medical work:
                                                                                        • Part 1 refers to requirements and testing of
■    Soft, comfortable and flexible                                                       gloves for freedom from holes
■    High sensitivity                                                                   • Part 2 refers to requirements and tests for
■    Clean and anti-static                                                                physical properties
                                                                                        • Part 3 refers to requirements and tests for
■    Ambidextrous                                                                         biological evaluation
                                                                                        • Part 4 refers to requirements and testing
Q U A L I T Y S TA N DA R D &
                                                                                          for shelf life determination
T E S T I N G C E R T I F I C AT I O N S
■    FDA 510(k) registered
■    ISO 13485 & ISO 9001:2015
■    EN 455 & EN374
■    Chemotherapy Drug rated per ASTM 6978
■    CE
E X P I R AT I O N DAT E
■ 5 years from date of manufacture

PAC K AG I N G I N F O R M AT I O N
■    100 gloves per box
■    10 boxes/1000 gloves per case
■    Box dimensions: 235 x 125 x 68mm
■    Case dimensions: 365 x 265 x 255mm

36          F R O N T L I N E C R O S S I N G S ™ M E D I C A L S U P P LY LT D .
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FL-GLV2

VINYL EXAM GLOVES
(POWDER FREE)

                    Actual packaging may vary by market.
PRODUCT DESCRIPTION                                                                  PAC K AG I N G I N F O R M AT I O N

■    Disposable vinyl gloves for patient examination                                 ■ 100 gloves per box (box dimensions: 23.0cm x
■    Powder free                                                                        12.5cm x 6cm)
■    Transparent/clear colour
■    For single use only                                                             N A M E O F M A N U FAC T U R E R

                                                                                     ■ Shandong Intco Medical Products Co., Ltd.
M AT E R I A L / D I M E N S I O N S

■ Clear examination glove made of pure PVC                                           M A N U FAC T U R E R A D D R E S S
  plastics using a unique powderless process
                                                                                     ■ Qiwang Road, Naoshan Industrial Park,
■ 100% latex free
                                                                                        Qingzhou, Weifang, Shandong, China 262500
■ Cuff Length: 9” (230mm)
■ Available in 4 sizes:
  • Small, Medium, Large, X-Large                                                       What is CE?
                                                                                         CE marking is a certification mark that
                                                                                         indicates conformity with health, safety,
F E AT U R E S                                                                           and environmental protection standards for
■    Soft and uniform thickness                                                          products sold within the European Economic
                                                                                         Area (EEA). The CE marking is also found on
■    Ambidextrous with rolled rim                                                        products sold outside the EEA that have been
■    Anti-static and oil resistant                                                       manufactured to EEA standards.
■    High tensile properties and puncture resistance
                                                                                        What is ASTM D5250-06?
                                                                                         ASTM D5250 is a standardized laboratory
Q U A L I T Y S TA N DA R D &                                                            testing method that measures the quali-
                                                                                         ty of poly(vinyl chloride) gloves for medical
T E S T I N G C E R T I F I C AT I O N S
                                                                                         application. This test involves an evaluation
■ ASTM D5250-06                                                                          of freedom from holes, physical dimensions,
                                                                                         physical property characteristics, and powder
■ EN 455-1,2,3,4                                                                         residue for powder-free gloves.
■ MDALL License Number: 93781
■ CE                                                                                    What is EN455-1,2,3,4?
                                                                                         EN455 is a standardized testing method
■ Registered as a Class II medical device on                                             developed by the European Committee for
  Health Canada’s MDALL database under Li-                                               Standardization (CEN) to evaluate any glove
  cense Number 93781                                                                     that could be used for medical work:
                                                                                         • Part 1 refers to requirements and testing of
                                                                                           gloves for freedom from holes
E X P I R AT I O N DAT E                                                                 • Part 2 refers to requirements and tests for
                                                                                           physical properties
■ 5 years from production date                                                           • Part 3 refers to requirements and tests for
                                                                                           biological evaluation
                                                                                         • Part 4 refers to requirements and testing
                                                                                           for shelf life determination

                                                                                        What is MDALL?
                                                                                         The Medical Devices Bureau (Bureau) of the
                                                                                         Therapeutic Products Directorate, Health
                                                                                         Canada is the Canadian federal regulator
                                                                                         responsible for licensing medical devices in
                                                                                         accordance with the Food and Drugs Act and
                                                                                         Regulations and the Medical Devices Regu-
                                                                                         lations. The Bureau maintains a database of
                                                                                         all licensed Class II, III, and IV medical devices
                                                                                         offered for sale in Canada called the Medical
                                                                                         Devices Active Listing (MDALL).
8
  MDALL reference as VINI vinyl glove. Amended to the Synguard
trademark by way of Interim Order Application Number: 314376

38           F R O N T L I N E C R O S S I N G S ™ M E D I C A L S U P P LY LT D .
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Eye
                                                          Protection
40   F R O N T L I N E C R O S S I N G S ™ M E D I C A L S U P P LY
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                                                                     O NDT. L I N E C R O S S I N G S ™ M E D I C A L S U P P LY LT D .   40
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FL-PG02

MEDICAL ISOLATION
FACE SHIELD (WITH
HEAD STRAP)
MODEL MK-201
PRODUCT DESCRIPTION                                                     PAC K AG I N G I N F O R M AT I O N

■ 180-degree medical face shield with comfort                           ■ 1 face shield per package (package dimensions:
   foam layer and head strap                                                 29cm x 25cm)

M AT E R I A L / D I M E N S I O N S                                    N A M E O F M A N U FAC T U R E R

■ Durable polymer that can be disinfected                               ■ Shaanxi Miaokang Medical Technology
■ 29cm x 25cm                                                                Co., Ltd.

F E AT U R E S                                                          M A N U FAC T U R E R A D D R E S S

■ 180 degrees of protection                                             ■ No. 303, Building E4, West Yungu, Diaotai Su,
                                                                             Xixian, Shaanxi, China, 712000
■ Anti-fog and anti-glare
■ Anti-static
■ Transparent                                                                What is EN 166,167,168: 2001?
■ Multiple use (after proper disinfection)                                    EN 166:2001 is the European standard cov-
                                                                              ering the requirements for protective eye-
                                                                              wear. It is closely linked to EN 167:2001 and
                                                                              EN 168:2001 which specify the optical and
Q U A L I T Y S TA N DA R D &                                                 non-optical test methods.
T E S T I N G C E R T I F I C AT I O N S

■ EN 166:2001
■ EN 167:2001
■ EN 168:2001
■ CE

E X P I R AT I O N DAT E

■ 3 years from date of production

                                                                F R O N T L I N E C R O S S I N G S ™ M E D I C A L S U P P LY LT D .   42
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FL-PG01

MEDICAL PROTECTIVE
GOGGLES (WITH
HEAD STRAP)
MODEL R101
PRODUCT DESCRIPTION                                                                 PAC K AG I N G I N F O R M AT I O N

■ Medical protective googles with head strap                                        ■ 1 unit per package (package dimensions:
                                                                                       44cm x 19cm x 9cm)

M AT E R I A L / D I M E N S I O N S
                                                                                    N A M E O F M A N U FAC T U R E R
■ PVC frame, polycarbonate lens
■ 28.5cm x 17cm                                                                     ■ Hangzhou Retsing Eyewear Co., Ltd.

■ Latex free
                                                                                    M A N U FAC T U R E R A D D R E S S

F E AT U R E S                                                                      ■ 405 Building 1, Chenggong Shida Mansion,
                                                                                       Gongshu District, Hangzhou, Zhejiang
■ Transparent
                                                                                       Province, China
■ Re-usable
■ Anti fog lens

                                                                                       What is 166,167,168: 2001?
                                                                                        EN 166:2001 is the European standard cov-
Q U A L I T Y S TA N DA R D &                                                           ering the requirements for protective eye-
T E S T I N G C E R T I F I C AT I O N S                                                wear. It is closely linked to EN 167:2001 and
                                                                                        EN 168:2001 which specify the optical and
■ FDA Registered                                                                        non-optical test methods.
■ EN 166:2001
                                                                                       What is GB14866-2066?
■ EN 167:2001                                                                           GB14866-2006 is a national testing standard
■ EN 168:2001                                                                           of the People’s Republic of China defining
                                                                                        required protective specifications of person-
■ GB14866-2066                                                                          al eye-protectors such as goggles and face
■ ANSI/ISEAZ87.1-2015                                                                   masks.

■ CE                                                                                   What is ANSI/ISEAZ87.1-2015?
                                                                                        ANSI/ISEA Z87.1-2015 prescribes the design,
                                                                                        performance specifications, and marking
                                                                                        of safety eye and face products, includ-
E X P I R AT I O N DAT E
                                                                                        ing millions of safety goggles, spectacles,
■ 3 years from date of production date                                                  face shields, and welding helmets, worn by
                                                                                        workers in thousands of manufacturing and
   (see packaging)                                                                      processing facilities, university and research
                                                                                        laboratories, and other occupational settings.
                                                                                        It was developed by the Z87 Committee on
                                                                                        Safety Eye and Face Protection, which is ad-
                                                                                        ministered by the International Safety Equip-
                                                                                        ment Association (ISEA), and approved by the
                                                                                        American National Standards Institute (ANSI).

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ANSI/AAMI PB 70:12 classification of barrier performance of surgical gowns, other
               protective apparel, surgical drapes and drape accessories:

 Level               Test                    Liquid Challenge                   Result                 Expected Barrier Effectiveness

         AATCC 42 Impact                                                                          Minimal water resistance (some
     1                                     Water                          ≤ 4.5 g
         Penetration                                                                              resistance to water spray)

         AATCC 42 Impact                                                                          Low water resistance (resistant to
                                           Water                          ≤ 1.0 g
         Penetration                                                                              water spray and some resistance to
     2
         AATCC 127                                                                                water penetration under constant
                                           Water                          ≥ 20 cm                 contact with increasing pressure)
         Hydrostatic Pressure

         AATCC 42 Impact                                                                          Moderate water resistance (resistant
                                           Water                          ≤ 1.0 g
         Penetration                                                                              to water spray and some resistance
     3
         AATCC 127                                                                                to water penetration under constant
                                           Water                          ≥ 50 cm                 contact with increasing pressure)
         Hydrostatic Pressure

         ASTM F1670
                                                                          no penetration
         Synthetic Blood                   Surrogate
                                                                          at 2 psi
         Penetration Test                  Blood
                                                                          (13.8 kPa)
         (for surgical drapes)
                                                                                                  Blood and viral penetration
     4
         ASTM F1671 Viral                                                                         resistance (2 psi)
                                                                          no penetration
         Penetration Test                  Bacteriophage
                                                                          at 2 psi
         (for surgical and                 Phi-X174
                                                                          (13.8 kPa)
         isolation gowns)

                                                                Protective
                                                                  Clothing
46       F R O N T L I N E C R O S S I N G S ™ M E D I C A L S U P P LY
                                                                     F R LT
                                                                         O NDT. L I N E C R O S S I N G S ™ M E D I C A L S U P P LY LT D .   46
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FL-PI03

NON-SURGICAL
ISOLATION GOWN
ANSI/AAMI PB70:2012
(LEVEL 3)
PRODUCT DESCRIPTION                                                                 E X P I R AT I O N DAT E

■ Non-surgical isolation gown                                                       ■ 3 years from date of production date (see
■ Meets the standard of ANSI/AAMI                                                      packaging)
  PB70:2012 (LEVEL 3)
■ Non-sterile                                                                       PAC K AG I N G I N F O R M AT I O N

■ Blue colour                                                                       ■ 1 gown per package (package dimensions:
■ For single use only                                                                 30cm x 35cm)
                                                                                    ■ 50 gowns per carton (carton dimensions:
                                                                                      60cm x 38cm x 36cm)
M AT E R I A L / D I M E N S I O N S

■ Non-woven fabric PP+PE
                                                                                    N A M E O F M A N U FAC T U R E R

GLY II hanging type specification (cm)                                              ■ Zhejiang Baiyi Intelligent Garment Co., Ltd.

 ½ neck                                    27                                       M A N U FAC T U R E R A D D R E S S
 Sleeve length                             92                                       ■ No. 1 Fengshan 1 Road Industrial Park, Hangbu
 Shoulder width                            66                                          Town, Kecheng, Quzhou, Zhejiang, China
 ½ bust                                    73
 ½ cuff                                    9
 Clothing length                           115                                         What is ANSI/AAMI PB70:2012?
                                                                                        This standard establishes a system of clas-
                                                                                        sification for protective apparel and drapes
                                                                                        used in health care facilities based on their
F E AT U R E S                                                                          liquid barrier performance and specifies re-
                                                                                        lated labeling requirements and standardized
■ Meets the standard of ANSI/AAMI PB70:2012
                                                                                        test methods for determining compliance.
   (LEVEL 3) liquid barrier performance and
   classification of protective apparel and drapes                                     What is AATCC 127-2018?
   intended for use in health care facilities:                                          AATCC 127 Hydrostatic Pressure Test mea-
                                                                                        sures the resistance of a fabric to the pene-
  • Rated pass on AATCC 127-2018 static hydro-                                          tration of water under hydrostatic pressure. It
    static resistance                                                                   is applicable to all types of fabrics, including
                                                                                        those treated with a water resistant or water
  • Rated pass on AATCC 42-2017 water-proof                                             repellent finish.
    property
                                                                                       What is AATCC 42-2017?
■ Ties at the back of the neck and waist
                                                                                        AATCC 42-2017 measures water resistance for
■ Extra length on waist ties                                                            any textile fabric which may or may not have
                                                                                        been given a water-resistant or water-repel-
                                                                                        lent finish. The test measures the resistance
                                                                                        of fabrics to the penetration of water by
Q U A L I T Y S TA N DA R D &                                                           impact.
T E S T I N G C E R T I F I C AT I O N S

■ ANSI/AAMI PB70:2012 (LEVEL 3)
■ AATCC 127-2018
■ AATCC 42-2017
■ CE

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FL-PI01

NON-SURGICAL
ISOLATION GOWN ANSI/
AAMI PB70:2012 (LEVEL 1)
PRODUCT DESCRIPTION                                                                 ■ 3 years from date of production date
■ Non-surgical isolation gown
■ Meets the standard of ANSI/AAMI                                                   PAC K AG I N G I N F O R M AT I O N
  PB70:2012 (LEVEL 1)                                                               ■ 1 gown per package (package dimensions:
■ Non-sterile                                                                         26cm x 38cm)
■ Blue colour                                                                       ■ 50 gowns per carton (carton dimensions:
■ For single use only                                                                 60cm x 38cm x 36cm)

                                                                                    N A M E O F M A N U FAC T U R E R
M AT E R I A L / D I M E N S I O N S

■ Non-woven fabric PP+PE                                                            ■ Shandong Baihuashen Biotechnology Technol-
                                                                                       ogy Co., Ltd.
GLY II hanging type specification (cm)
                                                                                    M A N U FAC T U R E R A D D R E S S
 ½ neck                                    27                                       ■ 1st Floor Factory Building, Building 10, SME
 Sleeve length                             92                                          Industrialization Base, Biomedical Park, 1777
 Shoulder width                            66                                          Dazheng Road, High-Tech Zone, Jinan City,
 ½ bust                                    73                                          Shandong Province, China
 ½ cuff                                    9
 Clothing length                           115

                                                                                       What is ANSI/AAMI PB70:2012?
                                                                                        This standard establishes a system of clas-
F E AT U R E S
                                                                                        sification for protective apparel and drapes
■ Meets the standard of ANSI/AAMI PB70:2012                                             used in health care facilities based on their
     (LEVEL 1) liquid barrier performance and                                           liquid barrier performance and specifies re-
                                                                                        lated labeling requirements and standardized
     classification of protective apparel and drapes                                    test methods for determining compliance.
     intended for use in health care facilities:
                                                                                       What is AATCC 127-2018?
     • Rated pass on AATCC 127-2018 static                                              AATCC 127 Hydrostatic Pressure Test mea-
       hydrostatic resistance                                                           sures the resistance of a fabric to the pene-
     • Rated pass on AATCC 42-2017 water-proof                                          tration of water under hydrostatic pressure. It
                                                                                        is applicable to all types of fabrics, including
       property                                                                         those treated with a water resistant or water
■ Ties at the back of the neck and waist                                                repellent finish.

■ Extra length on waist ties                                                           What is AATCC 42-2017?
                                                                                        AATCC 42-2017 measures water resistance for
                                                                                        any textile fabric which may or may not have
                                                                                        been given a water-resistant or water-repel-
Q U A L I T Y S TA N DA R D &                                                           lent finish. The test measures the resistance
T E S T I N G C E R T I F I C AT I O N S                                                of fabrics to the penetration of water by
                                                                                        impact.
■ ANSI/AAMI PB70:2012 (LEVEL 1)
■ AATCC 127-2018
■ AATCC 42-2017
■ CE

E X P I R AT I O N DAT E

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FL-PI02

NON-SURGICAL
ISOLATION GOWN ANSI/
AAMI PB70:2012 (LEVEL 2)
PRODUCT DESCRIPTION                                                                 E X P I R AT I O N DAT E

■ Non-surgical isolation gown                                                       ■ 3 years from date of production date
■ Meets the standard of ANSI/AAMI
  PB70:2012 (LEVEL 2)
                                                                                    PAC K AG I N G I N F O R M AT I O N
■ Non-sterile
■ Blue colour                                                                       ■ 1 gown per package (package dimensions:
                                                                                      26cm x 38cm)
■ For single use only
                                                                                    ■ 50 gowns per carton (carton dimensions:
                                                                                      60cm x 38cm x 36cm)
M AT E R I A L / D I M E N S I O N S

■ Non-woven fabric PP+PE
                                                                                    N A M E O F M A N U FAC T U R E R

GLY II hanging type specification (cm)                                              ■ Shandong Baihuashen Biotechnology Technol-
                                                                                       ogy Co., Ltd.
 ½ neck                                    27
 Sleeve length                             92
                                                                                    M A N U FAC T U R E R A D D R E S S
 Shoulder width                            66
                                                                                    ■ 1st Floor Factory Building, Building 10, SME
 ½ bust                                    73
                                                                                       Industrialization Base, Biomedical Park, 1777
 ½ cuff                                    9                                           Dazheng Road, High-Tech Zone, Jinan City,
 Clothing length                           115                                         Shandong Province, China

F E AT U R E S
                                                                                       What is ANSI/AAMI PB70:2012?
■ Meets the standard of ANSI/AAMI PB70:2012                                             This standard establishes a system of clas-
     (LEVEL 2) liquid barrier performance and                                           sification for protective apparel and drapes
     classification of protective apparel and drapes                                    used in health care facilities based on their
                                                                                        liquid barrier performance and specifies re-
     intended for use in health care facilities:                                        lated labeling requirements and standardized
     • Rated pass on AATCC 127-2018 static                                              test methods for determining compliance.
       hydrostatic resistance                                                          What is AATCC 127-2018?
     • Rated pass on AATCC 42-2017 water-proof                                          AATCC 127 Hydrostatic Pressure Test mea-
                                                                                        sures the resistance of a fabric to the pene-
       property
                                                                                        tration of water under hydrostatic pressure. It
■ Ties at the back of the neck and waist                                                is applicable to all types of fabrics, including
                                                                                        those treated with a water resistant or water
■ Extra length on waist ties                                                            repellent finish.

                                                                                       What is AATCC 42-2017?
                                                                                        AATCC 42-2017 measures water resistance for
Q U A L I T Y S TA N DA R D &
                                                                                        any textile fabric which may or may not have
T E S T I N G C E R T I F I C AT I O N S                                                been given a water-resistant or water-repel-
                                                                                        lent finish. The test measures the resistance
■ ANSI/AAMI PB70:2012 (LEVEL 2)
                                                                                        of fabrics to the penetration of water by
■ AATCC 127-2018                                                                        impact.
■ AATCC 42-2017
■ CE

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FL-PI04

SINGLE-USE MEDICAL
PROTECTIVE CLOTHING
(EN14605 TYPE 4)
PRODUCT DESCRIPTION                                                                 E X P I R AT I O N DAT E

■ Disposable full-body medical protective cloth-                                    ■ 2 years from date of production
     ing (hooded)
■    Tested compliant to EN 14126:2003/AC:2004                                      PAC K AG I N G I N F O R M AT I O N
     standards                                                                      ■ 1 gown per package (package dimensions:
■    Tested compliant to EN 14605:2005+A1:2009                                         26cm x 38cm)
     standards (Type 4)
■    Non-sterile
■    Single use

M AT E R I A L / D I M E N S I O N S

■ Non-woven inner layer material with polypro-
     pylene outer film
Sizing Information (cm)

        Model #                    Length                    Bust             Sleeve length           Arm Cuff            Foot Cuff
          160                         165                     120                      84                 18                 24
           165                       169                      125                      86                 18                 24
           170                        173                     130                      90                 18                 24
           175                        178                     135                      93                 18                 24
          180                         181                     140                      96                 18                 24
           185                       188                      145                      99                 18                 24

F E AT U R E S                                                                      N A M E O F M A N U FAC T U R E R

■ Elastics on all cuffs                                                             ■ Zhejiang Baiyi Intelligent Garment Co., Ltd.
■ Hooded design
■ High quality zipper                                                               M A N U FAC T U R E R A D D R E S S

■ Breathable SMS material with double layer                                         ■ No. 1 Fengshan 1 Road Industrial Park, Hangbu
     protection                                                                        Town, Kecheng, Quzhou, Zhejiang, China

Q U A L I T Y S TA N DA R D &
T E S T I N G C E R T I F I C AT I O N S

■ FDA Establishment Registration
■ Tested compliant to EN 14126:2003/AC:2004
     standards
                                                         EN 14605:2005+A1:2009 (Type 4)                        EN 14126:2003/AC:2004
 Abrasion Resistance                                                  No Classification
 Compression-Folding (Schildknecht)
                                                                            Class 6
 Flex Cracking Resistance
 Trapezoidal Tear Resistance                                                 Class 1                             Referring to Type 4
 Tensile Strength                                                            Class 1                                 comment
 Puncture Resistance                                                        Class 2
 Seam Strength                                                              Class 4
 Whole Suit Testing                                                           Pass

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Protective
 Clothing Accessories

56   F R O N T L I N E C R O S S I N G S ™ M E D I C A L S U P P LY
                                                                  F RLT
                                                                     O NDT. L I N E C R O S S I N G S ™ M E D I C A L S U P P LY LT D .   56
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FL-ACE1

DISPOSABLE
BOUFFANT
HEAD COVER
MODEL STYLE NO. 175
PRODUCT DESCRIPTION                                                                 N A M E O F M A N U FAC T U R E R
■ Disposable medical bouffant head cover                                            ■ Zhejiang Baiyi Intelligent Garment Co., Ltd.
■ Non-sterile
■ Single use
                                                                                    M A N U FAC T U R E R A D D R E S S

                                                                                    ■ No. 1 Fengshan 1 Road Industrial Park, Hangbu
M AT E R I A L / D I M E N S I O N S                                                   Town, Kecheng, Quzhou, Zhejiang, China
■ 32cm x 15cm

F E AT U R E S
                                                                                       What is EN 14126:2003/AC:2004?
■ Elastic headband for secure fit                                                       This European Standard specifies require-
                                                                                        ments and test methods for re-usable and
                                                                                        limited use protective clothing providing
                                                                                        protection against infective agents. Clothing
Q U A L I T Y S TA N DA R D &                                                           worn by surgical teams or drapes laid on pa-
T E S T I N G C E R T I F I C AT I O N S                                                tients to prevent cross-contamination during
                                                                                        surgical interventions are not covered by the
■ FDA Establishment Registration                                                        scope of this standard.
■ ISO9001:2015
                                                                                       What is ISO9001:2015?
■ EN 14126:2003/AC:2014                                                                 ISO 9001 is defined as the international stan-
                                                                                        dard that specifies requirements for a quality
                                                                                        management system (QMS). Organizations
E X P I R AT I O N DAT E                                                                use the standard to demonstrate the ability
                                                                                        to consistently provide products and services
■ 2 years from date of production                                                       that meet customer and regulatory require-
                                                                                        ments.

PAC K AG I N G I N F O R M AT I O N

■ 50-unit box (package dimensions:
     32cm x 36cm

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FL-ACE2

DISPOSABLE
MEDICAL ISOLATION
SHOE COVER
PRODUCT DESCRIPTION                                                                 N A M E O F M A N U FAC T U R E R
■ Disposable medical isolation shoe cover                                           ■ Shandong Haidike Medical Products Co., Ltd.
■ Non-sterile
■ Single use
                                                                                    M A N U FAC T U R E R A D D R E S S

                                                                                    ■ Tianfu Road, Dongcheng District, Shan County,
M AT E R I A L / D I M E N S I O N S                                                   Heze City, Shandong Province, China
■ Non-woven fabric
■ One-size fits all

                                                                                       What is EN 14126:2003?
F E AT U R E S                                                                          This European Standard specifies require-
                                                                                        ments and test methods for re-usable and
■ Elastic foot cuff for a more secure fit                                               limited use protective clothing providing
■ Treads on sole for better traction                                                    protection against infective agents. Clothing
                                                                                        worn by surgical teams or drapes laid on pa-
                                                                                        tients to prevent cross-contamination during
                                                                                        surgical interventions are not covered by the
Q U A L I T Y S TA N DA R D &                                                           scope of this standard.
T E S T I N G C E R T I F I C AT I O N S

■ FDA Establishment Registration
■ CE
■ EN ISO 13485:2016
■ EN 14126:2003
■ EN ISO 10993-10
■ ISO 9073-3-1989
■ ISO 22609
■ EN 1041:2008
■ EN ISO 14971:2012

E X P I R AT I O N DAT E

■ 3 years from date of production

PAC K AG I N G I N F O R M AT I O N

■ 2-unit package (package dimensions:
  30 cm x 22cm
■ 100-unit carton (carton dimensions:
  60cm x 38cm x 36cm)

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Thermometers

62   F R O N T L I N E C R O S S I N G S ™ M E D I C A L S U P P LY
                                                                  F RLT
                                                                     O NDT. L I N E C R O S S I N G S ™ M E D I C A L S U P P LY LT D .   62
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FL-THM2

INFRARED
FOREHEAD
THERMOMETER
MODEL DET-306
PRODUCT DESCRIPTION                                                                 N A M E O F M A N U FAC T U R E R
■ “Non-touch” type infrared forehead                                                ■ Joytech Healthcare Co., Ltd.
   thermometer

                                                                                    M A N U FAC T U R E R A D D R E S S
M AT E R I A L / D I M E N S I O N S
                                                                                    ■ No.365, Wuzhou Road, Yuhang Economic
■ Battery-powered “non-touch” infrared                                                 Development Zone, Hangzhou City, Zhejiang
  forehead thermometer                                                                 Province, 311100, China
■ 15.3cm x 4.1cm x 4.4cm

F E AT U R E S

■ Backlit display
■ 10 set memory values
■ Fahrenheit and Celsius readings
■ Battery powered (2 x AAA)
■ Temperature measuring range:
   10o C – 40o C (50o F – 104o F)

Q U A L I T Y S TA N DA R D &
T E S T I N G C E R T I F I C AT I O N S

■ Registered as a Class II medical device on
  Health Canada’s MDALL database under Li-
  cense Number: 104622
■ CE

E X P I R AT I O N DAT E

■ 3 years from date of production

PAC K AG I N G I N F O R M AT I O N

■ 1-unit per package (package dimensions:
   17cm x 9cm x 5cm)

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Syringes & Needles

66   F R O N T L I N E C R O S S I N G S ™ M E D I C A L S U P P LY
                                                                  F RLT
                                                                     O NDT. L I N E C R O S S I N G S ™ M E D I C A L S U P P LY LT D .   66
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FL-NDL01

SAFETY HYPODERMIC
NEEDLE – 25G X 1”
PRODUCT DESCRIPTION                                                                 PAC K AG I N G I N F O R M AT I O N

■ Precision ultra-sharp needle with Safety Shield                                   ■ 100 safety needles per box
    ensures optimal protection from sharps injuries                                 ■ 10 boxes per case
■   Hinged protective shield is easy to activate with
    one hand (finger, thumb or surface method)
                                                                                    N A M E O F M A N U FAC T U R E R
■   Audible click and visual indicator confirm
    safety mechanism is activated and covers                                        ■ Wuxi Yushou Medical Appliances Co, Ltd.
    entire needle cannula for added protection                                         (Yeso-med)
■   Safety shield can be pushed back to allow clear
    view of injection site
                                                                                    M A N U FAC T U R E R A D D R E S S
■   ISO color coded for easy gauge identification
                                                                                    ■ Xigang Road, Dongbeitang, Wuxi, Jiangsu
■   Fits any brand of syringe
                                                                                       Province, China
■   Sterile and disposable for single patient use
■   25 Gauge x 1” length (other sizes available)

M AT E R I A L / D I M E N S I O N S

■ Plastic hub with Luer Lock connection
■ Stainless Steel, regular wall, regular bevel
  needle
■ Sterile, non-toxic, non-pyrogenic
■ No Natural Rubber Latex
■ 25 Gauge x 1” length (other sizes available)

F E AT U R E S

■ Regular bevel hypodermic needle with safety
  shield
■ Hinged protective shield
■ Luer Lock connection
■ Sterile and disposable for single patient use

Q U A L I T Y S TA N DA R D &
T E S T I N G C E R T I F I C AT I O N S

■ ISO color coded for easy gauge identification

E X P I R AT I O N DAT E

■ 10 years from date of manufacture

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