Duoderm 403333

by Convatec, Purchasing Department

Duoderm 403333 is a Class I device made by Convatec, Purchasing Department, listed in FDA GUDID since 12 Apr 2019 (UDI-DI 00768455107278), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00768455107278 UDI-DI	Date12 Apr 2019Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00768455107278

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Duoderm
Generic name: Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial
Model / reference: 403333

Primary DI / UDI-DI: 00768455107278
FDA product code: NAD
GMDN term: Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial

Device class: Class I
Regulation number: 878.4020
GUDID distribution status: In Commercial Distribution

Size: Length — 20.00000 Centimeter
Width — 23.00000 Centimeter

Similar devices in this category

Other devices filed under Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial.

Other devices from Convatec, Purchasing Department

Cure Medical K2

Class II
Sur-Fit Natura 401557

Class I
Esteem 423652

Class I
Esteem+ 413510

Class I

See all devices from Convatec, Purchasing Department →

Properties

Supplied sterile
Single use
Over-the-counter
Premarket exempt
Lot / batch number
Expiration date

Other properties (9, all answered No)