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Kendall

FDA UDI

Class I (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Kendall FDA UDI
Generic Name
Synthetic polymer semi-permeable film dressing, adhesive FDA UDI
Device Name
Transparent Film Dressing,Moisture Vapor Permeable FDA UDI
Model / Reference
6651 FDA UDI
Description
Transparent Film Dressing,Moisture Vapor Permeable FDA UDI

Identifiers

Catalog Number
6651 FDA UDI
Primary DI / UDI-DI
10884521007314 FDA UDI
FDA Product Code
NAD FDA UDI
GMDN Term
Synthetic polymer semi-permeable film dressing, adhesive FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 1.50 Inch FDA UDI
Width — 1.50 Inch FDA UDI

Category: Synthetic polymer semi-permeable film dressing, adhesive

Kendall by Cardinalhealth — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Synthetic polymer semi-permeable film dressing, adhesive.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 281977b0-d965-4691-84f2-f782fc6a2756 37 fields · synced May 30, 2026