An invasive, distal component of an electrosurgical assembly intended to deliver electrosurgical current in a bipolar configuration (i.e., without a return electrode) to tissues for cutting/coagulation/ablation during endoscopic (e.g., laparoscopic, arthroscop
| Company | Devices | Share |
|---|---|---|
| Olympus Winter & Ibe Gmbh | 120 | 21% |
| Medline Industries, Inc. | 74 | 13% |
| Progressive Medical, Inc. | 66 | 11% |
| Livsmed | 45 | 8% |
| Depuy Mitek, Llc | 36 | 6% |
| Richard Wolf Gmbh | 33 | 6% |
| Ace Medical Devices Private Limited | 33 | 6% |
| Stryker Corporation | 24 | 4% |
| Merit Medical Systems, Inc. | 19 | 3% |
| Jiangsu Hope Biomedical Science&Technology Co.,Ltd. | 17 | 3% |
| Starmed Co.,Ltd | 16 | 3% |
| Dornier Medtech America, Inc. | 14 | 2% |
Company = labeler of record on GUDID. 32 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 | 231 |
| FAS | Electrode, Electrosurgical, Active, Urological | 165 |
| HIH | Hysteroscope (And Accessories) | 86 |
| FAS | ELECTRODE, ELECTROSURGICAL, ACTIVE, UROLOGICAL | 78 |
| GEI | Electrosurgical, cutting & coagulation & accessories | 76 |
| FJL | Resectoscope | 75 |
Use these as the dimensions to specify in a tender line.
585 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Endoscopic electrosurgical electrode, bipolar, single-use", from 32 companies. The largest labeler is Olympus Winter & Ibe Gmbh with 21% of records.
GEI (Electrosurgical, Cutting & Coagulation & Accessories), FAS (Electrode, Electrosurgical, Active, Urological), HIH (Hysteroscope (And Accessories)), FAS (ELECTRODE, ELECTROSURGICAL, ACTIVE, UROLOGICAL)
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.