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AmerisourceBergen 11404

by Bp Pharmaceuticals Laboratories Unlimited Company

AmerisourceBergen 11404 is a Class I device made by Bp Pharmaceuticals Laboratories Unlimited Company, listed in FDA GUDID since 11 Oct 2021 (UDI-DI 00368001114042), 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 Number00368001114042 UDI-DI Date11 Oct 2021ListedStatusListed 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  • Withdrawn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
AmerisourceBergen
Generic name
Absorbent underpad, non-antimicrobial, single-use
Model / reference
11404
Primary DI / UDI-DI
00368001114042
FDA product code
KME
GMDN term
Absorbent underpad, non-antimicrobial, single-use
Device class
Class I
Regulation number
880.6060
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KME (Bedding, Disposable, Medical).

Other devices from Bp Pharmaceuticals Laboratories Unlimited Company

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Properties

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