Comfeel Plus Transparent 33536

by Coloplast A/S

Comfeel Plus Transparent 33536 is a Class I device made by Coloplast A/S, listed in FDA GUDID since 11 Mar 2022 (UDI-DI 05708932641616), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number05708932641616 UDI-DI	Date11 Mar 2022Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 05708932641616

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Comfeel Plus Transparent
Generic name: Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial
Model / Ref / Catalog: 33536

Primary DI / UDI-DI: 05708932641616
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 — 5 Inch
Width — 9 Centimeter
Length — 14 Centimeter
Width — 3.5 Inch

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Properties

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

Other properties (9, all answered No)