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Contiplex® 339237

by B. Braun Medical, Inc.

Contiplex® 339237 is a Class II device made by B. Braun Medical, Inc., listed in FDA GUDID since 23 Mar 2025 (UDI-DI 04046961000099), 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 Number04046961000099 UDI-DI Date23 Mar 2025ListedStatusListed 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  • Withdrawn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
Contiplex®
Generic name
Peripheral anaesthesia catheter set, non-medicated
Model / Ref / Catalog
339237
Primary DI / UDI-DI
04046961000099
FDA product code
CAZ
GMDN term
Peripheral anaesthesia catheter set, non-medicated
Device class
Class II
Regulation number
868.5140
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Related devices

Category: Peripheral anaesthesia catheter set, non-medicated

Similar devices

Other devices filed under FDA product code CAZ (Anesthesia conduction kit).

Other devices from B. Braun Medical, Inc.

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

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (8, all answered No)