A rigid combined electrosurgical handpiece and bipolar electrode, intended to deliver electrosurgical current from a system generator directly to tissues for cutting/coagulation during an open surgical procedure. It is available in a variety of forms (e.g., pe
| Company | Devices | Share |
|---|---|---|
| Stingray Surgical Products L.L.C. | 3,939 | 32% |
| Kirwan Surgical Products Llc | 1,580 | 13% |
| Avalign Technologies, Inc. | 875 | 7% |
| Günter Bissinger Medizintechnik Gmbh | 845 | 7% |
| Aspen Surgical Products, Inc. | 760 | 6% |
| Ambler Surgical Corp. | 586 | 5% |
| Elmed Incorporated | 572 | 5% |
| Titan Manufacturing Inc | 498 | 4% |
| Adeor Medical Ag | 310 | 2% |
| Novo Surgical, Inc. | 295 | 2% |
| Accurate Surgical & Scientific Instruments Corporation | 272 | 2% |
| Aesculap, Inc. | 195 | 2% |
Company = labeler of record on GUDID. 60 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 | 9,997 |
| GEI | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES | 2,195 |
| GEI | Electrosurgical, cutting & coagulation & accessories | 1,339 |
| GCJ | Laparoscope, General & Plastic Surgery | 147 |
| GCJ | Laparoscope, general & plastic surgery | 110 |
| BWA | Unit, Electrosurgical Andcoagulation, With Accessories | 100 |
Use these as the dimensions to specify in a tender line.
12,497 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Open-surgery electrosurgical handpiece/electrode, bipolar, reusable", from 60 companies. The largest labeler is Stingray Surgical Products L.L.C. with 32% of records.
GEI (Electrosurgical, Cutting & Coagulation & Accessories), GEI (ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES), GEI (Electrosurgical, cutting & coagulation & accessories), GCJ (Laparoscope, General & Plastic Surgery)
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.