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Contiplex® 339227

by B. Braun Medical, Inc.

Listed FDA GUDID listing, not in commercial distribution

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04046955130399 UDI-DI Date6 Mar 2023ListedStatusListed GUDID: not in commercial distribution

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  • Withdrawn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
339227
Primary DI / UDI-DI
04046955130399
FDA Product Code
CAZ
GMDN Term
Peripheral anaesthesia catheter set, non-medicated
Device Class
Class II
Regulation Number
868.5140
GUDID distribution status
Not in Commercial Distribution
MRI Safety
MR Unsafe

Other devices from B. Braun Medical, Inc.

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Convenience Kit
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No