Becker Systems

Edms 27931 Becker GS Tubing Smartsites

Registry build 21.09.26
5manufacturers in China registered for this device type
1catalogue number
1510(k) clearance

Who Else Makes It

Concentrated in Guangdong (3), Shanghai (2). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code GWM
Manufacturer City Province Registered as Device types
Shanghai Medical Instruments (Group) Ltd. Corp. Shanghai Shanghai Contract manufacturer 235
Amphenol Alden Products Company Shenzhen Guangdong Contract manufacturer 24
PAN-International Precision Electronic Co., Ltd. Dongguan Guangdong Contract manufacturer 4
Shenzhen Mindray BIO-Medical Electronics Co., Ltd. Shenzhen Guangdong Specification developer 61
Shanghai Wilpower Industrial Co., Ltd. Shanghai Shanghai Exporter 33

Record

Regulatory record for Becker Systems
Listed by Medtronic PS Medical, United States
FDA product code GWM
Device type Device, Monitoring, Intracranial Pressure
Device class Class 2
Regulation 21 CFR 882.1620
Record published 2024-06-23
Record revised 2024-12-23 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number

Catalogue Numbers

Catalogue numbers for Becker Systems
Catalogue number Size Status
27931 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Licox® GMS, Gesellschaft für medizinische Sondentechnik mbH 38
Sophysa Sophysa 32
Becker® Medtronic PS Medical 31
Codman Cerenovus, Inc. 29
Device, Monitoring, Intracranial Pressure Medtronic PS Medical 28
Exacta™ Medtronic PS Medical 28
Braincare Braincare Desenvolvimento E Inovacao Tecnologica SA 24
Camino® Integra Lifesciences (Ireland) Limited 20
Codman® Integra LifeSciences Production Corporation 19
Integra® Integra Lifesciences (Ireland) Limited 17
Aura Branchpoint & Aura Development LLC 17
Natus Natus Medical Incorporated 15

Showing 12 of 133. All products under Device, Monitoring, Intracranial Pressure

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K983799 1999-01-26

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