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Abena 1000021322

by Abena North America, Inc.

Abena 1000021322 is a Class I device made by Abena North America, Inc., listed in FDA GUDID since 8 Aug 2022 (UDI-DI 05713571000861), 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

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05713571000861 UDI-DI Date8 Aug 2022ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Abena
Generic name
Adult nappy
Model / reference
1000021322
Primary DI / UDI-DI
05713571000861
FDA product code
EYQ
GMDN term
Adult nappy
Device class
Class I
Regulation number
876.5920
GUDID distribution status
In Commercial Distribution

Related devices

Category: Adult nappy

Similar devices

Other devices filed under FDA product code EYQ (Garment, Protective, For Incontinence).

Other devices from Abena North America, Inc.

See all devices from Abena North America, Inc. →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)