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FDA UDI

Class I (US FDA UDI)

by Sempermed Usa, Inc.

Identity

Trade Name
force black FDA UDI
Generic Name
Nitrile examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
Device Name
Nitrile Exam Glove, size XL FDA UDI
Model / Reference
BKNF105 FDA UDI
Description
Nitrile Exam Glove, size XL FDA UDI

Identifiers

Catalog Number
BKNF105 FDA UDI
Primary DI / UDI-DI
00841277108637 FDA UDI
FDA Product Code
LZA FDA UDI
LZC FDA UDI
OPJ FDA UDI
QDO 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

force black 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 776e67a4-ddf5-4b09-9014-4e17cc6acf2b 35 fields · synced Jun 1, 2026