Myoguide System Model 8008

The Intronix Model 8008 Myoguide system (Myoguide) is a medical device that operates as an electromyography (EMG) amplifier with onboard stimulator and signal display. It is intended for…

Registry build 21.09.26

The Intronix Model 8008 Myoguide system (Myoguide) is a medical device that operates as an electromyography (EMG) amplifier with onboard stimulator and signal display. It is intended for use to amplify muscle signals (EMG) from muscle and provide audio and visual feedback to assist clinicians in locating areas of muscle activity. The stimulator can be used for nerve localization or to invoke a muscle twitch. These features provide feedback used for guidance of injections into muscle or in the vicinity of nerves. This device is a battery powered, handheld, EMG amplifier with audio feedback and stimulator, LCD EMG signal and device status display, and current stimulation ranging from 0 mA – 20 mA.

2manufacturers in China registered for this device type
1catalogue number
1510(k) clearance

Who Else Makes It

Concentrated in Jiangsu (1), Guangdong (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code BXN
Manufacturer City Province Registered as Device types
Suzhou Meccan Import and Export Corp. Suzhou Jiangsu Contract manufacturer 71
Easymed Instruments Co., Ltd. Daliang, Shunde, Foshan Guangdong Contract manufacturer 8

Record

Regulatory record for Myoguide System Model 8008
Listed by Intronix Technologies Corp., United States
FDA product code BXN
Device type Stimulator, Nerve, Battery-Powered
Device class Class 2
Regulation 21 CFR 868.2775
Premarket notification Exempt
Record published 2016-09-23
Record revised 2018-04-25 (version 3)

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 Myoguide System Model 8008
Catalogue number Size Status
8008 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
SunMed SunMed Group Holdings, LLC 22
Xavant Technology Xavant Technology (PTY) Ltd 14
Stimuplex® B. Braun Medical Inc. 12
AincA® Anesthesia Associates, Inc. 9
Halyard Avanos Medical, Inc. 8
Avanos Avanos Medical, Inc. 8
Stimpod Xavant Technology (PTY) Ltd 6
Multistim Vario Pajunk Gmbh Medizintechnologie 6
Multistim Sensor Pajunk Gmbh Medizintechnologie 5
MultiStim ECO Pajunk Gmbh Medizintechnologie 4
MultiStim Sensor PatientCable Pajunk Gmbh Medizintechnologie 4
Temena Temena GmbH 2

Showing 12 of 19. All products under Stimulator, Nerve, Battery-Powered

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K111985 2011-12-30

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