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Duoderm

FDA UDI

Class I (US FDA UDI)

by Convatec, Purchasing Department

Identity

Trade Name
DUODERM FDA UDI
Generic Name
Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial FDA UDI
Device Name
DuoDERM® CGF® EXtra Thin Dressing - 3" x 3" FDA UDI
Model / Reference
187901 FDA UDI
Description
DuoDERM® CGF® EXtra Thin Dressing - 3" x 3" FDA UDI

Identifiers

Primary DI / UDI-DI
00768455102785 FDA UDI
FDA Product Code
NAD FDA UDI
GMDN Term
Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial 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

No

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 — 7.5 Centimeter FDA UDI
Length — 7.5 Centimeter FDA UDI

Category: Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial

Duoderm by Convatec, Purchasing Department — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7d7275f5-9929-4cf7-b36b-e01834a6213d 35 fields · synced May 30, 2026