Consulting Wallah › Device Explorer › Equipment & monitoring › Electroencephalographic monitoring system
Device Explorer · FDA GUDID · GMDN 38736

Electroencephalographic monitoring system

An electrically-powered device assembly designed to continuously measure the electrical signals produced by a patient's brain and display/record them as an electroencephalogram (EEG) to evaluate brain function, typically in an examination room or intensive car

US‑registered devices94in commercial distribution
Companies10labelers on GUDID
Single‑use4%of device records
Sterile1%labelled sterile
Prescription88%Rx‑only share
ShareLinkedIn

Share of device records

Neuralynx, Inc.2729%
Epiminder Limited2527%
Neuroelectrics Barcelona Sl2223%
Moberg Research Inc77%
Eemagine Medical Imaging Solutions Gmbh44%
Mt Monitortechnik Gmbh & Co. Kg33%
Pascall Systems, Inc.33%
Xltek11%

Top labelers

CompanyDevicesShare
Neuralynx, Inc.2729%
Epiminder Limited2527%
Neuroelectrics Barcelona Sl2223%
Moberg Research Inc77%
Eemagine Medical Imaging Solutions Gmbh44%
Mt Monitortechnik Gmbh & Co. Kg33%
Pascall Systems, Inc.33%
Xltek11%
General Sleep11%
Prolira B.V.11%

Company = labeler of record on GUDID. 10 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Narcotrend Patient leadNarcotrend-Compact MPegasusATLAS Neurophysiology SystemPASCALL SYSTEMS, INC.ATLAS WorkstationATLAS Workstation MonitorPegasus Software License 512chPegasus Software License 480chPegasus Software License 448chPegasus Software License 416chPegasus Software License 384chPegasus Software License 352chPegasus Software License 320chPegasus Software License 288chPegasus Software License 256ch

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

FDA product codes

CodeNameDevices
GWQFull-Montage Standard Electroencephalograph45
OMCReduced- Montage Standard Electroencephalograph35
SEMSub-Scalp Implanted Electroencephalogram System For Remote P25
GWLAmplifier, Physiological Signal23
OLTNon-Normalizing Quantitative Electroencephalograph Software17
ORTBurst Suppression Detection Software For Electroencephalogra8

GMDN & GCC registration

  • GMDN code 38736 · non‑implantable
  • Single‑use 4% · sterile 1% · Rx‑only 88% · 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

Width (Inch) · 1Height (Inch) · 1

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

No closely related category with 50+ devices.

How many electroencephalographic monitoring system products are registered in the US?

94 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Electroencephalographic monitoring system", from 10 companies. The largest labeler is Neuralynx, Inc. with 29% of records.

Which FDA product codes apply?

GWQ (Full-Montage Standard Electroencephalograph), OMC (Reduced- Montage Standard Electroencephalograph), SEM (Sub-Scalp Implanted Electroencephalogram System For Remote P), GWL (Amplifier, Physiological Signal)

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.

How do I get quotes?

Add electroencephalographic monitoring system to the RFQ basket or use the form below with quantity, specification and delivery location; the Network returns comparable quotes from verified suppliers in 2–5 working days.

Request quotes for Electroencephalographic monitoring system

Hospitals, pharmacies and distributors anywhere: tell us what you need and the Consulting Wallah Network returns comparable quotes from verified suppliers. No fee for buyers.

Buying electroencephalographic monitoring system for a hospital group?Free executive assessment: we benchmark your prices and tender structure against the Network.
Book the free assessment

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.

Get quotes →