Magstim Single 90mm Standard Coil

Catalogue number 3193-00, listed by THE Magstim Company Ltd., United Kingdom, under Stimulator, Electrical, Evoked Response. 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shandong (1), Shaanxi (1), Guangdong (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code GWF
Manufacturer City Province Registered as Device types
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Xian Friendship Medical Electronics Co., Ltd. Xi’An Shaanxi Contract manufacturer 10
Shenzhen Launch Electrical Co., Ltd. Shenzhen Guangdong Contract manufacturer 8

Record

Regulatory record for Magstim Single 90mm Standard Coil
Listed by THE Magstim Company Ltd., United Kingdom
FDA product code GWF
Device type Stimulator, Electrical, Evoked Response
Device class Class 2
Regulation 21 CFR 882.1870
Establishment Complaint-file establishment, Manufacturer
Record published 2016-09-23
Record revised 2018-03-29 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for Magstim Single 90mm Standard Coil
Catalogue number Size Status
3193-00 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Stimulator, Electrical, Evoked Response Inomed Medizintechnik Gmbh 170
Alpine BioMed Alpine Biomed Aps 132
Natus Natus Neurology Incorporated 98
Keypoint Natus Manufacturing Limited 44
Stimulator, Electrical, Evoked Response Nihon Kohden America, Inc. 41
Stimulator, Electrical, Evoked Response Nihon Kohden Corp. 38
Powerease™ Instruments Medtronic Sofamor Danek, Inc. 36
Stimulator, Electrical, Evoked Response Stryker Leibinger Gmbh & Co. KG 29
Natus Xltek 27
Isis Inomed Medizintechnik Gmbh 26
Xltek Xltek 24
Natus Neurology Natus Neurology Incorporated 20

Showing 12 of 121. All products under Stimulator, Electrical, Evoked Response

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K130403 2013-08-23
K080499 2008-12-08
K051864 2005-12-21

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