An electrically-powered pedal used by an operator of a medical device to regulate the activation and/or intensity of a parent device (e.g., electrosurgical system generator, laser, ophthalmic examination unit, dental drill/saw system control unit) to which it
| Company | Devices | Share |
|---|---|---|
| Erbe Elektromedizin Gmbh | 28 | 5% |
| Karl Storz Gmbh & Co. Kg | 24 | 5% |
| Maquet Gmbh | 23 | 4% |
| E.M.S. Electro Medical Systems S.A. | 20 | 4% |
| Conmed Corporation | 20 | 4% |
| Medtronic Xomed, Inc. | 15 | 3% |
| Medtronic, Inc. | 15 | 3% |
| Solta Medical | 14 | 3% |
| Olympus Medical Systems Corp. | 13 | 2% |
| Medtronic Powered Surgical Solutions | 13 | 2% |
| Covidien Lp | 13 | 2% |
| Stryker Corporation | 12 | 2% |
Company = labeler of record on GUDID. 113 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 | 105 |
| GEI | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES | 61 |
| GEI | Electrosurgical, cutting & coagulation & accessories | 33 |
| HRX | ARTHROSCOPE | 23 |
| FQO | TABLE, OPERATING-ROOM, AC-POWERED | 23 |
| ERL | DRILL, SURGICAL, ENT (ELECTRIC OR PNEUMATIC) INCLUDING HANDP | 20 |
Use these as the dimensions to specify in a tender line.
525 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Foot-switch, electrical", from 113 companies. The largest labeler is Erbe Elektromedizin Gmbh with 5% of records.
GEI (Electrosurgical, Cutting & Coagulation & Accessories), GEI (ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES), GEI (Electrosurgical, cutting & coagulation & accessories), HRX (ARTHROSCOPE)
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.