Contiplex® 339229

by B. Braun Medical, Inc.

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

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

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number04046955130436 UDI-DI	Date6 Mar 2023Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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Withdrawn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: 339229

Primary DI / UDI-DI: 04046955130436
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 Unsafe

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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