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Procure

FDA UDI

Class I (US FDA UDI)

by Twin Med, LLC

Identity

Trade Name
Procure FDA UDI
Generic Name
Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
Device Name
Powder Free Gloves, Latex, Exam, PF, Medium, 100ea/bx 10bx/cs FDA UDI
Model / Reference
PC202 FDA UDI
Description
Powder Free Gloves, Latex, Exam, PF, Medium, 100ea/bx 10bx/cs FDA UDI

Identifiers

Catalog Number
PC202 FDA UDI
Primary DI / UDI-DI
10840330701874 FDA UDI
FDA Product Code
LYY FDA UDI
GMDN Term
Hevea-latex 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial

Procure by Twin Med, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Twin Med, LLC

Sources (1)

  • FDA UDI d6f7a1f3-0485-4746-bb62-99eee3fa01fd 37 fields · synced Jun 1, 2026