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Customed 712057102984

by Customed, Inc.

Customed 712057102984 (9002984) is a Class I device made by Customed, Inc., listed in FDA GUDID since 10 Aug 2023 (UDI-DI M20890029842), 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 NumberM20890029842 UDI-DI Date10 Aug 2023ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Customed
Generic name
Adult nappy
Model / Ref / Catalog
712057102984, 9002984
Primary DI / UDI-DI
M20890029842
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 Customed, Inc.

See all devices from Customed, Inc. →

Properties

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