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Device Explorer · FDA GUDID · GMDN 58494

Electrosurgical return electrode, single-use

A dispersive conductor intended to be fastened to a patient and connected to an electrosurgical/radio-frequency ablation system generator, to allow return of electrical current from the patient to the generator during an electrosurgical procedure. It has a lar

US‑registered devices308in commercial distribution
Companies42labelers on GUDID
Single‑use97%of device records
Sterile2%labelled sterile
Prescription93%Rx‑only share
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Share of device records

Medimax Tech Inc.6421%
Nissha Medical Technologies Ltd5016%
3M Company268%
Conmed Corporation227%
Cathay Manufacturing Corp.176%
Bioprotech Inc.103%
Erbe Elektromedizin Gmbh93%
Covidien Lp93%

Top labelers

CompanyDevicesShare
Medimax Tech Inc.6421%
Nissha Medical Technologies Ltd5016%
3M Company268%
Conmed Corporation227%
Cathay Manufacturing Corp.176%
Bioprotech Inc.103%
Erbe Elektromedizin Gmbh93%
Covidien Lp93%
Aspen Surgical Products, Inc.83%
Medico Electrodes International Limited83%
Nikomed Usa83%
Medline Industries, Inc.83%

Company = labeler of record on GUDID. 42 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

CathayCATHAYNAN/ANeuroTherm™ERBEArthrex®BovieDynamic DIAGNOSTICS, INCMediSourceNet, IncGrounding PadsNeutral PlateOWLEpimedRF Disposable Grounding PadMediMax Tech

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

FDA product codes

CodeNameDevices
GEIElectrosurgical, Cutting & Coagulation & Accessories205
GEIELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES81
GEIElectrosurgical, cutting & coagulation & accessories38
GXDGenerator, lesion, radiofrequency4
JOSElectrode, Electrosurgical3
GXIProbe, radiofrequency lesion2

GMDN & GCC registration

  • GMDN code 58494 · non‑implantable
  • Single‑use 97% · sterile 2% · 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

Area/Surface Area (Square centimeter) · 8Length (Feet) · 7Length (Inch) · 3Width (Inch) · 3

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

How many electrosurgical return electrode, single-use products are registered in the US?

308 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Electrosurgical return electrode, single-use", from 42 companies. The largest labeler is Medimax Tech Inc. with 21% of records.

Which FDA product codes apply?

GEI (Electrosurgical, Cutting & Coagulation & Accessories), GEI (ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES), GEI (Electrosurgical, cutting & coagulation & accessories), GXD (Generator, lesion, radiofrequency)

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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