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Telfa

FDA UDI

Class I (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Telfa FDA UDI
Generic Name
Adhesive bandage FDA UDI
Device Name
Adhesive Island Dressing FDA UDI
Model / Reference
7539LF FDA UDI
Description
Adhesive Island Dressing FDA UDI

Identifiers

Catalog Number
7539LF FDA UDI
Primary DI / UDI-DI
10884527021925 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Adhesive bandage FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5240 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
Width — 2 Inch FDA UDI
Length — 3.75 Inch FDA UDI

Category: Adhesive bandage

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

Similar devices

Also classified as Adhesive bandage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 9ea50e1c-0b55-46e1-8a6a-be9aef926d5f 37 fields · synced Jun 8, 2026