ADVANCE IF 51CF

Primary DI
00810120951225
Brand
ADVANCE IF 51CF
Company
Diamond Gloves
Model
NCF-51S
Device description
Powder Free Black Nitrile Examination Gloves, Chemo Tested & Fentanyl Protection, SMALL
Published
2023-06-22
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
false
Single use
true

Product Codes#

Code, Name table
CodeName
LZAPolymer Patient Examination Glove

Product Code Classifications#

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

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00810120951225PackageGS110In Commercial Distribution
00810120951218PrimaryGS10
00810120951201Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00810120951225008101209512258101209512250810120951225
00810120951218008101209512188101209512180810120951218
00810120951201008101209512018101209512010810120951201

GMDN Terms#

Term, Definition table
TermDefinition
Nitrile examination/treatment glove, non-powdered, non-antimicrobialA device made of nitrile 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 patient/staff against contaminants and risk of allergy to latex. It will have appropriate characteristics regarding tactility and comfort of use, and should provide appropriate physical properties (e.g., tensile strength, resistance to puncture, elasticity), and uniformity of dimensions (i.e., sizing consistency). This is a single-use device.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
052262122
Device count
100
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
true
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00810120952253ADVANCE IF 36BPF-36XS2025-05-30
00810120952284ADVANCE IF 36BPF-36S2025-05-30
00810120952314ADVANCE IF 36BPF-36M2025-05-30
00810120952345ADVANCE IF 36BPF-36L2025-05-30
00810120952376ADVANCE IF 36BPF-36XL2025-05-30
00810120952406ADVANCE IF 36BPF-36XXL2025-05-30
00810120952437ADVANCE IF 42BPF-42M2025-07-01
00810120952468ADVANCE IF 42BPF-42XS2025-07-01
00810120952499ADVANCE IF 42BPF-42S2025-07-01
00810120952529ADVANCE IF 42BPF-42L2025-07-01
00810120952550ADVANCE IF 42BPF-42XL2025-07-01
00810120952581ADVANCE IF 42BPF-42XXL2025-07-01
00810120952444ADVANCE IF 42BPF-42M2025-07-01
00810120952475ADVANCE IF 42BPF-42XS2025-07-01
00810120952505ADVANCE IF 42BPF-42S2025-07-01
00810120952536ADVANCE IF 42BPF-42L2025-07-01
00810120952567ADVANCE IF 42BPF-42XL2025-07-01
00810120952598ADVANCE IF 42BPF-42XXL2025-07-01
00810120952260ADVANCE IF 36BPF-36XS2025-05-30
00810120952420ADVANCE IF 36BPF-36S2025-05-30

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