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Kendall

FDA UDI

Class I (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
Kendall FDA UDI
Generic Name
First aid absorbent pad/bandage FDA UDI
Device Name
Blue Washcloths 9-3/8 x 13-1/2 in. (23.8 x 34.3 cm) Moderate FDA UDI
Model / Reference
6360 FDA UDI
Description
Blue Washcloths 9-3/8 x 13-1/2 in. (23.8 x 34.3 cm) Moderate FDA UDI

Identifiers

Catalog Number
6360 FDA UDI
Primary DI / UDI-DI
20192253040002 FDA UDI
FDA Product Code
FRL FDA UDI
GMDN Term
First aid absorbent pad/bandage FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5300 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: First aid absorbent pad/bandage

Kendall by Cardinal Health 200, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as First aid absorbent pad/bandage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 84f0f4ce-516a-4391-b92d-e0770c4630bd 34 fields · synced Jun 8, 2026