← Back to catalogue

Telfa

FDA UDI

Class I (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Telfa FDA UDI
Generic Name
Adhesive bandage FDA UDI
Device Name
Non-adherent Pad FDA UDI
Model / Reference
3279 FDA UDI
Description
Non-adherent Pad FDA UDI

Identifiers

Catalog Number
3279 FDA UDI
Primary DI / UDI-DI
10884521065376 FDA UDI
FDA Product Code
NAD FDA UDI
GMDN Term
Adhesive bandage 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 10 Inch FDA UDI
Width — 8 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 65398c51-2d15-49ce-8285-0364344c3a03 37 fields · synced May 30, 2026