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velvet 100

FDA UDI

Class I (US FDA UDI)

by Sempermed Usa, Inc.

Identity

Trade Name
velvet 100 FDA UDI
Generic Name
Nitrile examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
Device Name
velvet Nitrile Exam Glove PF, size M FDA UDI
Model / Reference
SMNS103 FDA UDI
Description
velvet Nitrile Exam Glove PF, size M FDA UDI

Identifiers

Catalog Number
SMNS103 FDA UDI
Primary DI / UDI-DI
00841277108163 FDA UDI
FDA Product Code
OPJ FDA UDI
LZA FDA UDI
QDO FDA UDI
LZC 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
Not 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

velvet 100 by Sempermed Usa, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sempermed Usa, Inc.

Sources (1)

  • FDA UDI 02a98764-ab9c-4e6e-bcec-0901499d8e7d 36 fields · synced Jun 6, 2026