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Telfa

FDA UDI

Class I (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Telfa FDA UDI
Generic Name
Synthetic polymer semi-permeable film dressing, adhesive FDA UDI
Device Name
Non-adherent Clear Wound Dressing FDA UDI
Model / Reference
1113 FDA UDI
Description
Non-adherent Clear Wound Dressing FDA UDI

Identifiers

Catalog Number
1113 FDA UDI
Primary DI / UDI-DI
20884521532578 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
Width — 12 Inch FDA UDI

Category: Synthetic polymer semi-permeable film dressing, adhesive

Telfa 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 c2c6bc45-eefe-4c38-83cc-ba5feb0f3db7 37 fields · synced May 30, 2026