Stimulator, Electrical, Evoked Response

LCD Stand (when mounting 2 LCD displays on the KD-030A)

Registry build 21.09.26
3manufacturers in China registered for this device type
38catalogue numbers in this listing
2510(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 Stimulator, Electrical, Evoked Response
Listed by Nihon Kohden Corp., Japan
FDA product code GWF
Device type Stimulator, Electrical, Evoked Response
Device class Class 2
Regulation 21 CFR 882.1870
Establishment Specification developer, Manufacturer
Record published 2016-09-05
Record revised 2024-04-15 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries lot or batch number, serial number

Catalogue Numbers

Catalogue numbers for Stimulator, Electrical, Evoked Response
Catalogue number Size Status
JW-120B In distribution
KH-231B In distribution
VD-403B In distribution
JB-232B In distribution
BM-230B In distribution
JB-316B In distribution
JS-201B In distribution
SEN-4100A In distribution
JB-132B In distribution
JS-101B In distribution
JS-203B In distribution
MS-230B In distribution
YB-201B In distribution
BM-412B In distribution
RY-230B In distribution
BM-121B In distribution
KH-122A In distribution
QI-120A In distribution
QP-101BK In distribution
JB-206B In distribution
JS-202B In distribution
JB-102B In distribution
JJ-230B In distribution
NE-432B In distribution
BM-122B In distribution
JB-212B In distribution
QP-260BK In distribution
NE-113A In distribution
JW-121B In distribution
DR-531B-14 In distribution
LS-102J In distribution
YE-103J In distribution
JS-210B In distribution
JB-101B In distribution
JB-210B In distribution
PV-230B In distribution
JB-116B In distribution
JS-204B 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
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
Pulse Nuvasive, Inc. 16

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
K142624 2015-04-24
K120397 2012-09-19

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