An instrument specifically designed to be used to check the calibration and performance of linear and non-linear medical accelerator systems used for radiation therapy applications, for quality assurance (QA) purposes. It includes a variety of instruments used
| Company | Devices | Share |
|---|---|---|
| Iba Dosimetry Gmbh | 77 | 45% |
| Sun Nuclear Corp. | 52 | 30% |
| Modus Medical Devices Inc | 11 | 6% |
| Ptw-Freiburg Physikalisch-Technische Werkstätten Dr. Pychlau Gmbh | 7 | 4% |
| Standard Imaging Inc. | 6 | 4% |
| Aktina Corp. | 5 | 3% |
| Medscint Inc. | 4 | 2% |
| Varian Medical Systems, Inc. | 2 | 1% |
| Scandidos Ab | 2 | 1% |
| Radiological Imaging Technology | 1 | 1% |
| Medtec, Inc. | 1 | 1% |
| Accuray Incorporated | 1 | 1% |
Company = labeler of record on GUDID. 14 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 |
|---|---|---|
| IYE | Accelerator, Linear, Medical | 116 |
| LHO | Instrument, Quality-Assurance, Radiologic | 52 |
| IXG | Phantom, Anthropomorphic, Radiographic | 13 |
| MWW | Accessory - Film Dosimetry System | 9 |
| LHN | System, Radiation Therapy, Charged-Particle, Medical | 1 |
| OUG | Medical device data system | 1 |
Use these as the dimensions to specify in a tender line.
171 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Accelerator system quality assurance device", from 14 companies. The largest labeler is Iba Dosimetry Gmbh with 45% of records.
IYE (Accelerator, Linear, Medical), LHO (Instrument, Quality-Assurance, Radiologic), IXG (Phantom, Anthropomorphic, Radiographic), MWW (Accessory - Film Dosimetry System)
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.