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Tri-Connector 472026

by B. Braun Medical, Inc.

Tri-Connector 472026 is a Class II device made by B. Braun Medical, Inc., listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04046964184635), 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 Number04046964184635 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  • Withdrawn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
Tri-Connector
Generic name
In-line backflow valve, single-use
Model / Ref / Catalog
472026
Primary DI / UDI-DI
04046964184635
FDA product code
FPA
GMDN term
In-line backflow valve, single-use
Device class
Class II
Regulation number
880.5440
GUDID distribution status
In Commercial Distribution

Related devices

Category: In-line backflow valve, single-use

Similar devices

Other devices filed under FDA product code FPA (Set, administration, intravascular).

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)