TwitchView™

Supporting infection control, TwitchView™ utilizes a single-patient use Electrode Array. With the flexibility to secure to either left or right hand in seconds, the Electrode Array is…

Registry build 21.09.26

Supporting infection control, TwitchView™ utilizes a single-patient use Electrode Array. With the flexibility to secure to either left or right hand in seconds, the Electrode Array is easily adopted into the pre-surgical workflow. The one-piece, auto-centering design mitigates placement errors → a common cause of intra-operative system failure and measurement inaccuracies.

5manufacturers in China registered for this device type
6catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (3), Jiangsu (1), Tianjin (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 KOI
Manufacturer City Province Registered as Device types
Amphenol Medical Technologies (Dongguan) Co., Ltd. Dongguan Guangdong Contract manufacturer 77
Shenzhen Launch Electrical Co., Ltd. Shenzhen Guangdong Contract manufacturer 8
Linxens Healthcare (Tianjin) Co., Ltd. Jinnan District Tianjin Contract manufacturer 7
Shenzhen Mindray BIO-Medical Electronics Co., Ltd. Shenzhen Guangdong Specification developer 61
GE Medical Systems (China) Co., Ltd. Wuxi Jiangsu Contract manufacturer 57

Record

Regulatory record for TwitchView™
Listed by Blink Device Company, United States
FDA product code KOI
Device type Stimulator, Nerve, Peripheral, Electric
Device class Class 2
Regulation 21 CFR 868.2775
Establishment Manufacturer
510(k) K172843
Record published 2018-09-05
Record revised 2020-02-06 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries serial number
Packaging Box of 25

Catalogue Numbers

Catalogue numbers for TwitchView™
Catalogue number Size Status
Charging Dock v1 In distribution
Monitor v1 In distribution
Cable Assembly v1 14′ In distribution
Cable Assembly v1 In distribution
Electrode v1 In distribution
Cable Assembly v1 12′ In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Stimulator, Nerve, Peripheral, Electric GE Healthcare Finland OY 7
WiTOF Idmed Corp. 6
Fisher & Paykel Healthcare Fisher & Paykel Healthcare, Ltd. 5
Halyard Avanos Medical, Inc. 5
Avanos Avanos Medical, Inc. 5
Smart Cable NMT Module and Accessories Nihon Kohden Corp. 4
Eye adapter TOF3D Mipm Mammendorfer Institut für Physik und Medizin GmbH 2
TetraSens Pediatric Senzime AB (Publ.) 2
Temperature sensor TOF3D Mipm Mammendorfer Institut für Physik und Medizin GmbH 2
TetraGraph Senzime AB (Publ.) 2
TetraSensitive Senzime AB (Publ.) 2
Thumb adapter TOF3D Mipm Mammendorfer Institut für Physik und Medizin GmbH 2

Showing 12 of 61. All products under Stimulator, Nerve, Peripheral, Electric

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K192958 2020-04-02
K172843 2018-03-29

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