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Pink Ribbon Polychlor Pf Exam

FDA UDI

Class I (US FDA UDI)

by Smart Health Llc

Identity

Trade Name
PINK RIBBON POLYCHLOR PF EXAM FDA UDI
Generic Name
Polychloroprene examination/treatment glove, non-powdered FDA UDI
Model / Reference
431042 FDA UDI

Identifiers

Catalog Number
431042 FDA UDI
Primary DI / UDI-DI
D7664310421 FDA UDI
FDA Product Code
LZA FDA UDI
GMDN Term
Polychloroprene examination/treatment glove, non-powdered 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

No

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: Polychloroprene examination/treatment glove, non-powdered

Pink Ribbon Polychlor Pf Exam by Smart Health Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Smart Health Llc

Sources (1)

  • FDA UDI b6dbf860-1401-449c-94dd-f2733c23b3b4 33 fields · synced Jun 1, 2026