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Device Explorer · FDA GUDID · GMDN 35723

Nerve-locating system

An multicomponent assembly of electrically-powered devices designed to locate a nerve by applying an electrical stimulus with a probe and observing muscle responses. Once the pathways are located, their transmission capabilities can be assessed by comparing ob

US‑registered devices287in commercial distribution
Companies19labelers on GUDID
Single‑use40%of device records
Sterile26%labelled sterile
Prescription80%Rx‑only share
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Share of device records

Medtronic Xomed, Inc.14751%
Medtronic Sofamor Danek, Inc.5820%
Avanos Medical, Inc.228%
Neurovision Medical Products, Inc.217%
Checkpoint Surgical, Inc.93%
Allotrope Medical Inc.52%
Aspen Surgical Products, Inc.52%
Medos International Sàrl52%

Top labelers

CompanyDevicesShare
Medtronic Xomed, Inc.14751%
Medtronic Sofamor Danek, Inc.5820%
Avanos Medical, Inc.228%
Neurovision Medical Products, Inc.217%
Checkpoint Surgical, Inc.93%
Allotrope Medical Inc.52%
Aspen Surgical Products, Inc.52%
Medos International Sàrl52%
Northgate Technologies Inc.31%
B. Braun Medical Inc.21%
Neo Medical Inc.21%
The Magstim Company Limited10%

Company = labeler of record on GUDID. 19 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Neurosign Mute SensorStimuplex® HNS 12NerveStim PureStimuplex®CARDINAL HEALTHN/AEvala nerve stimulatorNeuralytixStimSiteBovieThermi Peripheral Nerve StimulatorStimSite AM-VY1 AdapterStimSite Activation CardStimSite Signal BoxENT NIM ElectrodeNIM Vital

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 RESPONSE147
ETNSTIMULATOR, NERVE136
ETNStimulator, Nerve65
GWJSTIMULATOR, AUDITORY, EVOKED RESPONSE53
GWQFull-montage Standard Electroencephalograph53
IYNSystem, imaging, pulsed doppler, ultrasonic46

GMDN & GCC registration

  • GMDN code 35723 · non‑implantable
  • Single‑use 40% · sterile 26% · Rx‑only 80% · 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 (Millimeter) · 18Length (Meter) · 16Outer Diameter (Millimeter) · 7Needle Gauge (Gauge) · 4Length (Centimeter) · 3Length (Feet) · 3

Use these as the dimensions to specify in a tender line.

How many nerve-locating system products are registered in the US?

287 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Nerve-locating system", from 19 companies. The largest labeler is Medtronic Xomed, Inc. with 51% of records.

Which FDA product codes apply?

GWF (STIMULATOR, ELECTRICAL, EVOKED RESPONSE), ETN (STIMULATOR, NERVE), ETN (Stimulator, Nerve), GWJ (STIMULATOR, AUDITORY, EVOKED RESPONSE)

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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