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Pinnacle® 601231

by B. Braun Medical, Inc.

Pinnacle® 601231 is a Class II device made by B. Braun Medical, Inc., listed in FDA GUDID since 9 Mar 2019 (UDI-DI 04046955162185), 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 Number04046955162185 UDI-DI Date9 Mar 2019ListedStatusListed 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  • Withdrawn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
Pinnacle®
Generic name
Intravenous solution compounder
Model / Ref / Catalog
601231
Primary DI / UDI-DI
04046955162185
FDA product code
NEP
GMDN term
Intravenous solution compounder
Device class
Class II
Regulation number
880.5440
GUDID distribution status
In Commercial Distribution

Related devices

Category: Intravenous solution compounder

Other devices from B. Braun Medical, Inc.

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

Properties

  • Prescription use
  • Premarket exempt
  • Serial number
Other properties (12, all answered No)