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Pab® S5904-52

by B. Braun Medical, Inc.

Pab® S5904-52 is a Class II device made by B. Braun Medical, Inc., listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04046964187698), 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 Number04046964187698 UDI-DI Date23 Sep 2016ListedStatusListed 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  • Withdrawn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
Pab®
Generic name
Evacuated intravenous fluid container
Model / Ref / Catalog
S5904-52
Primary DI / UDI-DI
04046964187698
FDA product code
KPE
GMDN term
Evacuated intravenous fluid container
Device class
Class II
Regulation number
880.5025
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KPE (CONTAINER, I.V.).

Other devices from B. Braun Medical, Inc.

See all devices from B. Braun Medical, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)