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Abena 1999911722

by Abena North America, Inc.

Abena 1999911722 is a Class I device made by Abena North America, Inc., listed in FDA GUDID since 13 Oct 2025 (UDI-DI 05703538474507), 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

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05703538474507 UDI-DI Date13 Oct 2025ListedStatusListed 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  • Withdrawn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
1999911722
Primary DI / UDI-DI
05703538474507
FDA product code
EYQ
GMDN term
Adult nappy
Device class
Class I
Regulation number
876.5920
GUDID distribution status
In Commercial Distribution

Similar devices

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

Other devices from Abena North America, Inc.

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Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)