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Kimtech Sterling Nitrile Exam Gloves (s)

FDA UDI

Class I (US FDA UDI)

by Kimberly-Clark Global Sales, Inc.

Identity

Trade Name
KIMTECH STERLING NITRILE EXAM GLOVES (S) FDA UDI
Generic Name
Nitrile examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
Device Name
Examination Gloves FDA UDI
Model / Reference
50706 FDA UDI
Description
Examination Gloves FDA UDI

Identifiers

Catalog Number
50706-54 FDA UDI
Primary DI / UDI-DI
00036000507065 FDA UDI
510(k) Number
K161215 FDA UDI
FDA Product Code
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
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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nitrile examination/treatment glove, non-powdered, non-antimicrobial

Kimtech Sterling Nitrile Exam Gloves (s) by Kimberly-Clark Global Sales, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 98e80599-d505-4ab3-914c-865a7a69ef54 37 fields · synced Jun 1, 2026