Consulting Wallah › Device Explorer › Other devices › Electromyograph
Device Explorer · FDA GUDID · GMDN 11474

Electromyograph

An electrically-powered unit designed for the measurement and recording of the intrinsic electrical potential of skeletal muscle for display in the form of a graph [electromyograph (EMG)], typically for diagnosis of muscle and/or nerve disorders. It is designe

US‑registered devices343in commercial distribution
Companies15labelers on GUDID
Single‑use1%of device records
Sterile13%labelled sterile
Prescription95%Rx‑only share
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Share of device records

Natus Neurology Incorporated16448%
Xltek6419%
Natus Manufacturing Limited4613%
Cadwell Industries, Inc.288%
Eb Neuro Spa123%
Biometrics Limited103%
Bts Spa51%
Drive Devilbiss Healthcare41%

Top labelers

CompanyDevicesShare
Natus Neurology Incorporated16448%
Xltek6419%
Natus Manufacturing Limited4613%
Cadwell Industries, Inc.288%
Eb Neuro Spa123%
Biometrics Limited103%
Bts Spa51%
Drive Devilbiss Healthcare41%
Alpha Omega Engineering Co. Ltd.21%
Kinvent Biomecanique21%
Medical Measurement Systems B.V.21%
Alpine Biomed Aps10%

Company = labeler of record on GUDID. 15 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

NeuroOmega SystemAlpine BioMedSX230FW EMG SensorSX230-100 EMG SensorSX230-1000 EMG SensorFocusK MyoUrovalSierra SummitCascade IOMAXSierra Summit/AscentIOMAX AdapterIOMAX Extender PodDisposable Goggle FoamSierra WaveSierra II

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
GWFStimulator, Electrical, Evoked Response335
IKNElectromyograph, Diagnostic70
GWEStimulator, photic, evoked response34
JXEDEVICE, NERVE CONDUCTION VELOCITY MEASUREMENT34
IKNElectromyograph, diagnostic34
GWJSTIMULATOR, AUDITORY, EVOKED RESPONSE34

GMDN & GCC registration

  • GMDN code 11474 · non‑implantable
  • Single‑use 1% · sterile 13% · Rx‑only 95% · OTC 0%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Length (Inch) · 1

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How many electromyograph products are registered in the US?

343 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Electromyograph", from 15 companies. The largest labeler is Natus Neurology Incorporated with 48% of records.

Which FDA product codes apply?

GWF (Stimulator, Electrical, Evoked Response), IKN (Electromyograph, Diagnostic), GWE (Stimulator, photic, evoked response), JXE (DEVICE, NERVE CONDUCTION VELOCITY MEASUREMENT)

Is this the same as UAE/GCC registration?

No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.

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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.

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