Contiplex®

Contiplex® FX Non-Stimulating Tuohy Tray (Kit), 17Ga. x 3-1/2 in. Non-Stimulating Needle and Springwound Non-Stimulating Open Tip Catheter - Includes Ultrasound Transducer Cover and Gel…

Registry build 21.09.26

Contiplex® FX Non-Stimulating Tuohy Tray (Kit), 17Ga. x 3-1/2 in. Non-Stimulating Needle and Springwound Non-Stimulating Open Tip Catheter – Includes Ultrasound Transducer Cover and Gel (CNB350TKUFO)

1manufacturer
34catalogue numbers in this listing
7510(k) clearances naming this product code
1recall

Who Else Makes It

Registered in Jiangsu.

Chinese manufacturers registered for FDA product code CAZ
Manufacturer City Province Registered as Device types
Jiangsu Caina Medical Co., Ltd. Jiangyin Jiangsu Contract manufacturer 20

Record

Regulatory record for Contiplex®
Listed by B. Braun Medical Inc., United States
FDA product code CAZ
Device type Anesthesia Conduction Kit
Device class Class 2
Regulation 21 CFR 868.5140
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2017-03-04
Record revised 2020-04-27 (version 7)

Specifications

Specifications
MRI safety MR Unsafe
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Latex Labelled latex-free
Label carries lot or batch number, expiry date
Storage Handling environment temperature 1 to 40 °C; Storage environment temperature 20 to 25 °C
Distribution end date 2026-06-25

Catalogue Numbers

Catalogue numbers for Contiplex®
Catalogue number Size Per pack Status
331768 Gauge (cannula) : 18 10 In distribution
331758 Gauge (cannula) : 18 10 In distribution
331701 Gauge (cannula) : 18 10 In distribution
331691 Gauge (cannula) : 18 12 In distribution
333697 Gauge (cannula) : 25 5 In distribution
332127 10 In distribution
331698 Gauge (cannula) : 18 12 In distribution
331706 Gauge (cannula) : 18 10 In distribution
339237 Gauge (cannula) : 18 10 In distribution
332170 Gauge (Catheter) : 20 10 In distribution
331693 Gauge (Catheter) : 20 12 In distribution
331694 Gauge (Catheter) : 20 12 In distribution
339225 Gauge (Catheter) : 20 10 In distribution
331756 Gauge (cannula) : 18 10 In distribution
331695 Gauge (cannula) : 18 12 In distribution
331767 Gauge (cannula) : 18 10 In distribution
339229 Gauge (Catheter) : 20 10 In distribution
331766 Gauge (cannula) : 18 10 In distribution
331755 Gauge (Catheter) : 20 10 In distribution
339226 Gauge (Catheter) : 20 10 In distribution
339222 Gauge (cannula) : 18 12 In distribution
339223 Gauge (cannula) : 18 12 In distribution
339224 Gauge (Catheter) : 20 12 In distribution
339221 Gauge (cannula) : 18 12 In distribution
331757 Gauge (cannula) : 18 10 In distribution
331697 Gauge (cannula) : 18 12 Withdrawn
331763 Gauge (cannula) : 18 10 Withdrawn
331764 Gauge (Catheter) : 20 10 Withdrawn
339227 Gauge (cannula) : 18 10 Withdrawn
331761 Gauge (cannula) : 18 10 Withdrawn
331762 Gauge (Catheter) : 20 10 Withdrawn
331672 Gauge (Catheter) : 19 12 Withdrawn
332131 Gauge (Catheter) : 19 10 Withdrawn
331670 Gauge (Catheter) : 19 12 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Portex ICU Medical, Inc 1,340
Arrow Teleflex Medical LLC 508
Halyard Avanos Medical, Inc. 422
Avanos Avanos Medical, Inc. 315
Busse Hospital Disposables Robert Busse & Co., Inc. 215
Integra® Integra Pain Management 181
Epilong Pajunk Gmbh Medizintechnologie 79
BD Perisafe, BD Epilor, BD Luer-Lok Becton, Dickinson AND Company 44
Temena Temena GmbH 44
BD Luer-Lok, BD Glaspak Becton, Dickinson AND Company 36
Stimulong Sono Pajunk Gmbh Medizintechnologie 27
Clint Pharmaceuticals ICU Medical, Inc 26

Showing 12 of 109. All products under Anesthesia Conduction Kit

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K113059 2012-01-24
K090995 2009-08-14
K063282 2007-06-20
K033952 2004-02-04
K032144 2003-10-01
K971233 1997-10-17
K962696 1997-04-03

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity
2026-01-29 Class II Process control B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the p 210

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer