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Device Explorer · FDA GUDID · GMDN 35722

Block-monitoring peripheral nerve electrical stimulation system

An assembly of battery-powered devices designed to apply electrical stimuli to a peripheral nerve (e.g., the ulnar or lower extremity nerve) to assess the adequacy of neuromuscular block during surgery, and its reversal during the recovery period. The system t

US‑registered devices61in commercial distribution
Companies9labelers on GUDID
Single‑use15%of device records
Sterile0%labelled sterile
Prescription93%Rx‑only share
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Share of device records

Sunmed, Llc2236%
Senzime Ab (Publ.)1220%
Blink Device Company915%
Anesthesia Associates, Inc.915%
Mipm Mammendorfer Institut Für Physik Und Medizin Gmbh35%
Draeger Medical Systems, Inc.23%
Philips Medizin Systeme Böblingen Gmbh23%
Epsimed Llc12%

Top labelers

CompanyDevicesShare
Sunmed, Llc2236%
Senzime Ab (Publ.)1220%
Blink Device Company915%
Anesthesia Associates, Inc.915%
Mipm Mammendorfer Institut Für Physik Und Medizin Gmbh35%
Draeger Medical Systems, Inc.23%
Philips Medizin Systeme Böblingen Gmbh23%
Epsimed Llc12%
Nerbio Private Limited12%

Company = labeler of record on GUDID. 9 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

TetraHubTetraSensitiveTetraGraphTetraSens PediatricTetraSensTetraGraph XcomTetraGraph Philips InterfaceTetraGraph Pole Clamp kitTOF3D - Neuromuscular Transmission MonitorEPSIMEDMechanomyography Sensor (MMG) for Neuromuscular Infinity Trident Pod SystemInfinity Trident NMT SmartPodNMT cableNMT ModuleTwitchView™

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

FDA product codes

CodeNameDevices
KOIStimulator, Nerve, Peripheral, Electric28
BXNSTIMULATOR, NERVE, BATTERY-POWERED21
BXNStimulator, Nerve, Battery-Powered10
KOISTIMULATOR, NERVE, PERIPHERAL, ELECTRIC2

GMDN & GCC registration

  • GMDN code 35722 · non‑implantable
  • Single‑use 15% · sterile 0% · Rx‑only 93% · 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

No structured size data on the register.

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

No closely related category with 50+ devices.

How many block-monitoring peripheral nerve electrical stimulation system products are registered in the US?

61 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Block-monitoring peripheral nerve electrical stimulation system", from 9 companies. The largest labeler is Sunmed, Llc with 36% of records.

Which FDA product codes apply?

KOI (Stimulator, Nerve, Peripheral, Electric), BXN (STIMULATOR, NERVE, BATTERY-POWERED), BXN (Stimulator, Nerve, Battery-Powered), KOI (STIMULATOR, NERVE, PERIPHERAL, ELECTRIC)

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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