SW

Primary DI
00616489109754
Brand
SW
Company
SW SAFETY SOLUTIONS INC.
Model
L009205
Device description
TrueForm Latex Exam Gloves, Extra Large
Published
2021-10-19
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
OTC
true
Single use
true

Product Codes#

Code, Name table
CodeName
LYYLatex Patient Examination Glove

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LYYLatex Patient Examination GloveGeneral Hospital1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00616489109754PrimaryGS10
30616489109755Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00616489109754006164891097546164891097540616489109754
3061648910975530616489109755

GMDN Terms#

Term, Definition table
TermDefinition
Hevea-latex examination/treatment glove, non-powdered, non-antimicrobialA device made of Hevea natural rubber latex (NRL) intended as a protective barrier when worn on the hands of healthcare providers during patient examination/treatment or for other sanitary purposes; its inner surface is not covered with powder and it does not include antimicrobial agents/materials. The device is used mainly as a two-way barrier to protect both the patient and the staff against various contamination. It will have appropriate characteristics regarding tactility/comfort of use, and should provide appropriate physical properties (e.g., strength, elasticity), and uniformity of dimensions. This is a single-use device.

Regulatory Flags#

DUNS number
038152115
Device count
100
Lot or batch
true
Serial number
true
Manufacturing date on label
true
Contains natural rubber latex
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00616489004011SW K0004012021-11-04
00616489004028SWK0004022021-11-05
00616489004035SW K0004032021-11-05
00616489004042SW K0004042021-11-05
00616489004059SW K0004052021-11-05
00616489004066SW K0004062021-11-05
00616489100133SW N1253332021-10-22
00616489105619SW K0014012021-10-20
00616489105626SW K0014022021-10-20
00616489105633SW K0014032021-10-20
00616489105640SW K0014042021-10-20
00616489105657SW K0014052021-10-20
00616489125525SW K0714022021-10-22
00616489125532SW K0714032021-10-22
00616489125549SW K0714042021-10-22
00616489125556SW K0714052021-10-22
00616489125563SW K0714062021-10-22
00616489997528SW N9917522021-12-22
00616489997535SW N9917532021-12-22
30616489997529SW N9917522021-12-22

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
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10076490456549TOUCHNTUFFAnsell Healthcare ProductLYY2025-07-30
10076490456556TOUCHNTUFFAnsell Healthcare ProductLYY2025-07-30
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09555002101077AURELIA VIBRANTSUPERMAX GLOVE MANUFACTURING SDN. BHD.LYY2024-02-08
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09555002101411AURELIA DISTINCTSUPERMAX GLOVE MANUFACTURING SDN. BHD.LYY2024-02-08
09555002101428AURELIA DISTINCTSUPERMAX GLOVE MANUFACTURING SDN. BHD.LYY2024-02-08
09555002101435AURELIA DISTINCTSUPERMAX GLOVE MANUFACTURING SDN. BHD.LYY2024-02-08
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09555002101572AURELIA REFRESHSUPERMAX GLOVE MANUFACTURING SDN. BHD.LYY2024-02-08
09555002101589AURELIA REFRESHSUPERMAX GLOVE MANUFACTURING SDN. BHD.LYY2024-02-08
09555002101596AURELIA REFRESHSUPERMAX GLOVE MANUFACTURING SDN. BHD.LYY2024-02-08
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