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Device Explorer · FDA GUDID · GMDN 11500

Electrosurgical return electrode, single-use, sterile

A sterile 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 h

US‑registered devices53in commercial distribution
Companies10labelers on GUDID
Single‑use98%of device records
Sterile75%labelled sterile
Prescription40%Rx‑only share
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Share of device records

Zhejiang Shuyou Surgical Instrument Co.,Ltd.2751%
Cg Medtech Co.,Ltd.815%
Cathay Manufacturing Corp.48%
Cynosure, Llc36%
Gynex Corporation36%
Premier Dental Products Company24%
Soniquence, Llc24%
Deroyal Industries, Inc.24%

Top labelers

CompanyDevicesShare
Zhejiang Shuyou Surgical Instrument Co.,Ltd.2751%
Cg Medtech Co.,Ltd.815%
Cathay Manufacturing Corp.48%
Cynosure, Llc36%
Gynex Corporation36%
Premier Dental Products Company24%
Soniquence, Llc24%
Deroyal Industries, Inc.24%
Elmed Incorporated12%
Telea Electronic Engeenering Srl12%

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

Brand names on the register (sample)

cathayDisposable Grounding Pad SeriesELMEDEXTRA-LARGE GROUNDING PADNeutral PadPremierNeutral PlateDeRoyalEXTRA-LARGE GROUNDING PAD, 25 PCSPatient Dispersive PadPatient Dispercive PadL’DISQ®VESALIUS STERILE single-use neutral insulated pl

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 & Accessories37
GEIELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES10
ODRElectrosurgical patient return electrode3
ODRElectrosurgical Patient Return Electrode3

GMDN & GCC registration

  • GMDN code 11500 · non‑implantable
  • Single‑use 98% · sterile 75% · Rx‑only 40% · 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.

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

53 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, sterile", from 10 companies. The largest labeler is Zhejiang Shuyou Surgical Instrument Co.,Ltd. with 51% of records.

Which FDA product codes apply?

GEI (Electrosurgical, Cutting & Coagulation & Accessories), GEI (ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES), ODR (Electrosurgical patient return electrode), ODR (Electrosurgical Patient Return Electrode)

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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