Coaxial Airlock

413S150162

Registry build 21.09.26
5manufacturers in China registered for this device type
2catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Shanghai (1), Tianjin (1), Guangdong (1).

Chinese manufacturers registered for FDA product code MJG
Manufacturer City Province Registered as Device types
Shanghai KiNETIC Medical Co Ltd Shanghai Shanghai Contract manufacturer 19
Tianjin Newtrans Technology Development Tianjin Tianjin Exporter 11
Carbon (Shenzhen) Medical Device Co., Ltd. Shenzhen Guangdong Manufacturer 6
Ningbo Hicren Biotechnology Co., Ltd. Ningbo Zhejiang Manufacturer 5
Canyon Medical Inc. Nanjing Jiangsu Manufacturer 4

Record

Regulatory record for Coaxial Airlock
Listed by Pajunk Gmbh Medizintechnologie, Germany
FDA product code MJG
Device type Device, Percutaneous, Biopsy
Device class Class 1
Regulation 21 CFR 878.4800
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Private-label distributor, Complaint-file establishment, Manufacturer
510(k) K080674
Record published 2021-04-02
Record revised 2025-12-01 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Label carries lot or batch number, expiry date
Storage Storage environment humidity 10 to 65 % RH; Storage environment temperature 10 to 30 °C
Distribution end date 2025-06-17

Catalogue Numbers

Catalogue numbers for Coaxial Airlock
Catalogue number Size Per pack Status
413S150162 10 Withdrawn
413S150112 10 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Cardinal Health Cardinal Health 200, LLC 392
Cook Cook Incorporated 77
Intro M.D.L. S.R.L. 34
Franseen Cook Incorporated 32
HandCut M.D.L. S.R.L. 22
Turner Cook Incorporated 15
Palium Needle M.D.L. S.R.L. 14
Primocut Pajunk Gmbh Medizintechnologie 13
FastCutP M.D.L. S.R.L. 10
Co-Axial Cannula Bundle Argon Medical Devices, Inc. 10
Medline Industries, Inc. Medline Industries, Inc. 10
Greene Cook Incorporated 10

Showing 12 of 44. All products under Device, Percutaneous, Biopsy

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K080674 2008-05-09

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