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KIMGUARD™ KC100 Sterilization Wrap

FDA UDI

Class II (US FDA UDI)

by Kimberly-Clark Global Sales, Inc.

Identity

Trade Name
KIMGUARD™ KC100 Sterilization Wrap FDA UDI
Generic Name
Sterilization packaging, single-use FDA UDI
Device Name
45" x 45" Sterilization Wrap FDA UDI
Model / Reference
10745 FDA UDI
Description
45" x 45" Sterilization Wrap FDA UDI

Identifiers

Primary DI / UDI-DI
00036000107456 FDA UDI
FDA Product Code
FRG FDA UDI
GMDN Term
Sterilization packaging, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6850 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

No

FDA UDI

Category: Sterilization packaging, single-use

KIMGUARD™ KC100 Sterilization Wrap by Kimberly-Clark Global Sales, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sterilization packaging, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f0fb922a-e11c-4775-879e-0d3cfbe765e4 34 fields · synced Jun 1, 2026