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Telfa

FDA UDI

Class I (US FDA UDI)

by Cardinal Health 200, LLC

Identity

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

Identifiers

Catalog Number
1113 FDA UDI
Primary DI / UDI-DI
10192253045659 FDA UDI
FDA Product Code
NAD FDA UDI
GMDN Term
Synthetic polymer semi-permeable film dressing, wound-nonadherent 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
Length — 12 Inch FDA UDI

Category: Synthetic polymer semi-permeable film dressing, wound-nonadherent

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

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinal Health 200, LLC

Sources (1)

  • FDA UDI f95b9707-fa0c-44bd-b8fd-a90a225c4773 35 fields · synced Jun 8, 2026