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ProWorks

FDA UDI

Class I (US FDA UDI)

by Tranzonic Companies, The

Identity

Trade Name
ProWorks FDA UDI
Generic Name
Nitrile examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
Device Name
ProWorks® GrizzlyNite® Disposable Nitrile Exam Grade Gloves, Powder Free, Black, 5 mil, X-Large, 100/bx, 10 bxs/cs FDA UDI
Model / Reference
GL-N105FX FDA UDI
Description
ProWorks® GrizzlyNite® Disposable Nitrile Exam Grade Gloves, Powder Free, Black, 5 mil, X-Large, 100/bx, 10 bxs/cs FDA UDI

Identifiers

Catalog Number
GL-N105FX FDA UDI
Primary DI / UDI-DI
00075289122859 FDA UDI
FDA Product Code
LZA FDA UDI
GMDN Term
Nitrile examination/treatment glove, non-powdered, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6250 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nitrile examination/treatment glove, non-powdered, non-antimicrobial

ProWorks by Tranzonic Companies, The — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nitrile examination/treatment glove, non-powdered, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ca4d791b-db9f-49cb-8ea2-f22b7be0d7a9 35 fields · synced May 30, 2026