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Device Explorer · FDA GUDID · GMDN 61878

Inert gas-enhanced endoscopic electrosurgical electrode, single-use

An invasive, distal component of an inert gas-enhanced electrosurgical system intended to deliver electrosurgical current within a stream of inert gas [e.g., argon (Ar), helium (He)] directly to tissues for cutting/coagulation/ablation during an endoscopic (in

US‑registered devices62in commercial distribution
Companies5labelers on GUDID
Single‑use98%of device records
Sterile100%labelled sterile
Prescription97%Rx‑only share
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Share of device records

Erbe Elektromedizin Gmbh2744%
Conmed Corporation2235%
Olympus Winter & Ibe Gmbh711%
Us Medical Innovations, Llc35%
Covidien Lp35%

Top labelers

CompanyDevicesShare
Erbe Elektromedizin Gmbh2744%
Conmed Corporation2235%
Olympus Winter & Ibe Gmbh711%
Us Medical Innovations, Llc35%
Covidien Lp35%

Company = labeler of record on GUDID. 5 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

ErbeERBECanady Plasma GIT Side Fire ProbeCanady Plasma GIT ProbeABCABCFlex™, ABC®AVEOBEAMEROlympusValleylab

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 & ACCESSORIES30
GEIElectrosurgical, Cutting & Coagulation & Accessories29
GEIElectrosurgical, cutting & coagulation & accessories13

GMDN & GCC registration

  • GMDN code 61878 · non‑implantable
  • Single‑use 98% · sterile 100% · Rx‑only 97% · 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 (Meter) · 18Length (Millimeter) · 15Length (Centimeter) · 12Width (Millimeter) · 5Outer Diameter (Millimeter) · 4Length (Inch) · 2

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

How many inert gas-enhanced endoscopic electrosurgical electrode, single-use products are registered in the US?

62 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Inert gas-enhanced endoscopic electrosurgical electrode, single-use", from 5 companies. The largest labeler is Erbe Elektromedizin Gmbh with 44% of records.

Which FDA product codes apply?

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

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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