An invasive, distal component of an electrosurgical assembly intended to deliver electrosurgical current in a monopolar configuration (i.e., used with a patient contact return electrode) to tissues for cutting/coagulation/ablation during endoscopic (e.g., lapa
| Company | Devices | Share |
|---|---|---|
| Gimmi Gmbh | 281 | 17% |
| Steris Corporation | 199 | 12% |
| Avalign Technologies, Inc. | 164 | 10% |
| Karl Storz Gmbh & Co. Kg | 157 | 10% |
| Ab Medica | 130 | 8% |
| National Advanced Endoscopy Devices, Inc. | 117 | 7% |
| Encision, Inc. | 91 | 6% |
| Sontec Instruments, Inc. | 88 | 5% |
| Surgical Innovations Limited | 64 | 4% |
| Cameron-Miller Inc | 49 | 3% |
| Conmed Corporation | 39 | 2% |
| Surgical Direct, Inc. | 31 | 2% |
Company = labeler of record on GUDID. 38 companies in total; top 12 shown. Click headers to sort.
Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.
| Code | Name | Devices |
|---|---|---|
| GEI | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES | 554 |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | 391 |
| GCJ | Laparoscope, general & plastic surgery | 232 |
| GEI | Electrosurgical, cutting & coagulation & accessories | 195 |
| GCJ | Laparoscope, General & Plastic Surgery | 163 |
| FAS | ELECTRODE, ELECTROSURGICAL, ACTIVE, UROLOGICAL | 130 |
Use these as the dimensions to specify in a tender line.
1,641 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Endoscopic electrosurgical electrode, monopolar, reusable", from 38 companies. The largest labeler is Gimmi Gmbh with 17% of records.
GEI (ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES), GEI (Electrosurgical, Cutting & Coagulation & Accessories), GCJ (Laparoscope, general & plastic surgery), GEI (Electrosurgical, cutting & coagulation & accessories)
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.