Smart Cable NMT Module and Accessories

Neuro Muscular Transmission module

Registry build 21.09.26
5manufacturers in China registered for this device type
4catalogue numbers in this listing
3510(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 Smart Cable NMT Module and Accessories
Listed by Nihon Kohden Corp., Japan
FDA product code KOI
Device type Stimulator, Nerve, Peripheral, Electric
Device class Class 2
Regulation 21 CFR 868.2775
Establishment Specification developer, Manufacturer
Record published 2021-09-27
Record revised 2024-03-04 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date, serial number
Storage Storage environment temperature -10 to 40 °C; Storage environment humidity 15 to 95 % RH
Packaging Box of 10

Catalogue Numbers

Catalogue numbers for Smart Cable NMT Module and Accessories
Catalogue number Size Status
JW-201P In distribution
DH-101P In distribution
AF-201P In distribution
NM-345Y 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
TwitchView™ Blink Device Company 6
Fisher & Paykel Healthcare Fisher & Paykel Healthcare, Ltd. 5
Halyard Avanos Medical, Inc. 5
Avanos Avanos Medical, Inc. 5
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
K220976 2022-07-21
K213316 2021-12-29
K201949 2021-05-02

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