Telfa

FDA UDI

Class U (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name: Telfa FDA UDI
Generic Name: Non-woven gauze pad FDA UDI
Device Name: Telfa Antimicrobial Non-adherent Island Dressing 0.2 percent Polyhexamethylene Biguanide HCI (PHMB) Kills bacteria like Staph & MRSA AMD 4 x 10 in. (10.2 x 25.4 cm) FDA UDI
Model / Reference: 7667 FDA UDI
Description: Telfa Antimicrobial Non-adherent Island Dressing 0.2 percent Polyhexamethylene Biguanide HCI (PHMB) Kills bacteria like Staph & MRSA AMD 4 x 10 in. (10.2 x 25.4 cm) FDA UDI

Identifiers

Catalog Number: 7667 FDA UDI
Primary DI / UDI-DI: 10192253047486 FDA UDI
FDA Product Code: FRO FDA UDI
GMDN Term: Non-woven gauze pad FDA UDI

Classification

Device Class: U FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

Yes

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Length — 10 Inch FDA UDI
Width — 4 Inch FDA UDI

Category: Non-woven gauze pad

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class U	Pending data

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Manufacturer

Manufacturer: Cardinal Health 200, LLC

Sources (1)

FDA UDI 4d816e89-fbc6-4f90-bc6e-3caf8281460c 35 fields · synced Jun 8, 2026