← Back to catalogue

SafeHealth

FDA UDI

Class I (US FDA UDI)

by Pm Gloves U S A Inc

Identity

Trade Name
SafeHealth FDA UDI
Generic Name
Vinyl examination/treatment glove, non-powdered FDA UDI
Device Name
VINYL EXAMINATION GLOVES, Clear (S) FDA UDI
Model / Reference
SVF4C2 FDA UDI
Description
VINYL EXAMINATION GLOVES, Clear (S) FDA UDI

Identifiers

Catalog Number
SVF4C2 FDA UDI
Primary DI / UDI-DI
04712832880618 FDA UDI
FDA Product Code
LYZ FDA UDI
GMDN Term
Vinyl 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

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: Vinyl examination/treatment glove, non-powdered

SafeHealth by Pm Gloves U S A Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Pm Gloves U S A Inc

Sources (1)

  • FDA UDI 0b661180-6970-4c19-9319-3dd9b89a0920 36 fields · synced May 30, 2026