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Device Explorer · FDA GUDID · GMDN 61089

Nerve-locating system probe, single-use

A hand-held surgical instrument intended to function as an electrical conductor to locate a nerve during open surgery, and for diagnostic purposes [electromyography (EMG), cortical mapping], by delivering controlled electrical impulses to a specific body site

US‑registered devices360in commercial distribution
Companies17labelers on GUDID
Single‑use99%of device records
Sterile99%labelled sterile
Prescription79%Rx‑only share
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Share of device records

Technomed Engineering B.V.11031%
Xi'An Friendship Medical Electronics Co.,Ltd.5816%
Medtronic Xomed, Inc.3811%
Spes Medica Spa298%
Inomed Medizintechnik Gmbh288%
Neurovision Medical Products, Inc.288%
Koros U.S.A., Inc.134%
Surgentec, Llc123%

Top labelers

CompanyDevicesShare
Technomed Engineering B.V.11031%
Xi'An Friendship Medical Electronics Co.,Ltd.5816%
Medtronic Xomed, Inc.3811%
Spes Medica Spa298%
Inomed Medizintechnik Gmbh288%
Neurovision Medical Products, Inc.288%
Koros U.S.A., Inc.134%
Surgentec, Llc123%
Rhythmlink International, Llc123%
Spinal Elements82%
Medos International Sàrl62%
Tedan Surgical Innovations, L.L.C.51%

Company = labeler of record on GUDID. 17 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

LITeMapping Suction ProbeN/ANeuromonitoring KitALARA Neuro Access Needle KitTSIMedtronicIO-FLEXRhythmlink®NIM™NIMNIM-Spine®Hilger Dual-Stimulator Remote ProbeSilverstein Facial Nerve Stimulator Remote ProbeSurgical Probe, Monopolar w/Protected PlugSurgical Probe Monopolar

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

FDA product codes

CodeNameDevices
ETNStimulator, Nerve193
GXZElectrode, Needle156
ETNSTIMULATOR, NERVE46
GWFStimulator, Electrical, Evoked Response41
IKTElectrode, Needle, Diagnostic Electromyograph32
GXZELECTRODE, NEEDLE25

GMDN & GCC registration

  • GMDN code 61089 · non‑implantable
  • Single‑use 99% · sterile 99% · Rx‑only 79% · 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) · 35Outer Diameter (Millimeter) · 8Width (Millimeter) · 7Lumen/Inner Diameter (Millimeter) · 4Height (Millimeter) · 4Length (Centimeter) · 4

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

How many nerve-locating system probe, single-use products are registered in the US?

360 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Nerve-locating system probe, single-use", from 17 companies. The largest labeler is Technomed Engineering B.V. with 31% of records.

Which FDA product codes apply?

ETN (Stimulator, Nerve), GXZ (Electrode, Needle), ETN (STIMULATOR, NERVE), GWF (Stimulator, Electrical, 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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