A rigid tube designed to provide percutaneous (through the skin) tissue access through its lumen for an electrosurgical probe during radio-frequency (RF) ablation procedures (typically of peripheral nerves to treat chronic pain) and for the injection/aspiratio
| Company | Devices | Share |
|---|---|---|
| Diros Technology Inc | 263 | 29% |
| Avanos Medical, Inc. | 135 | 15% |
| Lccs Products Limited | 85 | 9% |
| Epimed International, Inc | 72 | 8% |
| Neurotherm, Inc. | 67 | 7% |
| St. Jude Medical, Inc. | 63 | 7% |
| Spectra Medical Devices, Llc | 49 | 5% |
| Cambridge Interventional Llc | 41 | 5% |
| Stryker Corporation | 34 | 4% |
| Medtronic Sofamor Danek, Inc. | 30 | 3% |
| Pajunk Gmbh Medizintechnologie | 25 | 3% |
| Stratus Medical Llc | 24 | 3% |
Company = labeler of record on GUDID. 16 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 |
|---|---|---|
| GXI | Probe, Radiofrequency Lesion | 647 |
| GXI | PROBE, RADIOFREQUENCY LESION | 322 |
| GXI | Probe, radiofrequency lesion | 149 |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | 44 |
| GEI | Electrosurgical, cutting & coagulation & accessories | 28 |
| GXD | Generator, lesion, radiofrequency | 13 |
Use these as the dimensions to specify in a tender line.
No closely related category with 50+ devices.
903 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Percutaneous radio-frequency ablation probe cannula, single-use", from 16 companies. The largest labeler is Diros Technology Inc with 29% of records.
GXI (Probe, Radiofrequency Lesion), GXI (PROBE, RADIOFREQUENCY LESION), GXI (Probe, radiofrequency lesion), 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.