A single- or double-lumen (coaxial) tube in a straight or spiral design intended to be used to conduct compressed surgical-grade air or nitrogen (N2) gas from a gas source, usually the central medical gas supply system, to a surgical drilling system or sawing
| Company | Devices | Share |
|---|---|---|
| De Soutter Medical Limited | 240 | 43% |
| Ohio Medical, Llc | 234 | 42% |
| Medtronic Powered Surgical Solutions | 31 | 6% |
| Aesculap Ag | 10 | 2% |
| Synthes Gmbh | 8 | 1% |
| Microaire Surgical Instruments Llc | 7 | 1% |
| Zimmer Orthopaedic Surgical Products, Inc. | 6 | 1% |
| Zimmer Surgical Sa | 6 | 1% |
| Adeor Medical Ag | 4 | 1% |
| Stryker Corporation | 2 | 0% |
| Conmed Corporation | 2 | 0% |
| Biomet Orthopedics, Llc | 1 | 0% |
Company = labeler of record on GUDID. 13 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 |
|---|---|---|
| GET | Motor, Surgical Instrument, Pneumatic Powered | 245 |
| BYX | TUBING, PRESSURE AND ACCESSORIES | 244 |
| HBB | MOTOR, DRILL, PNEUMATIC | 33 |
| HWE | INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCES | 13 |
| CAN | REGULATOR, PRESSURE, GAS CYLINDER | 12 |
| HSZ | Instrument, Surgical, Orthopedic, Pneumatic Powered & Access | 8 |
Use these as the dimensions to specify in a tender line.
552 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Pneumatic surgical power tool hose", from 13 companies. The largest labeler is De Soutter Medical Limited with 43% of records.
GET (Motor, Surgical Instrument, Pneumatic Powered), BYX (TUBING, PRESSURE AND ACCESSORIES), HBB (MOTOR, DRILL, PNEUMATIC), HWE (INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCES)
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.