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Accel® 622390

by B Braun Interventional Systems, Inc

Accel® 622390 is a Class I device made by B Braun Interventional Systems, Inc, listed in FDA GUDID since 16 Mar 2026 (UDI-DI 04046961018612), 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 Number04046961018612 UDI-DI Date16 Mar 2026ListedStatusListed 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  • Withdrawn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
Accel®
Generic name
Wearable adult urine collection bag, open-ended
Model / Ref / Catalog
622390
Primary DI / UDI-DI
04046961018612
FDA product code
FAQ
GMDN term
Wearable adult urine collection bag, open-ended
Device class
Class I
Regulation number
876.5250
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code FAQ (BAG, URINE COLLECTION, LEG, FOR EXTERNAL USE, STERILE).

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)