A device consisting of preserved human or animal tissue, or a two or three-dimensional (3-D) tissue-equivalent model designed to simulate the functional, physical, or a combination of these characteristics of normal or diseased human organs. It is available in
| Company | Devices | Share |
|---|---|---|
| L A P Gmbh Laser Applikationen | 159 | 50% |
| Ptw-Freiburg Physikalisch-Technische Werkstätten Dr. Pychlau Gmbh | 133 | 42% |
| Providus Holdings, Inc. | 13 | 4% |
| Scandidos Ab | 8 | 3% |
| Varian Medical Systems, Inc. | 2 | 1% |
Company = labeler of record on GUDID. 5 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 |
|---|---|---|
| LHO | Instrument, Quality-Assurance, Radiologic | 279 |
| IYE | Accelerator, Linear, Medical | 19 |
| IXG | Phantom, Anthropomorphic, Radiographic | 13 |
| IXG | Phantom, anthropomorphic, radiographic | 2 |
| LHN | System, Radiation Therapy, Charged-Particle, Medical | 2 |
Use these as the dimensions to specify in a tender line.
315 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Multi-modality therapeutic radiation phantom, anthropomorphic", from 5 companies. The largest labeler is L A P Gmbh Laser Applikationen with 50% of records.
LHO (Instrument, Quality-Assurance, Radiologic), IYE (Accelerator, Linear, Medical), IXG (Phantom, Anthropomorphic, Radiographic), IXG (Phantom, anthropomorphic, radiographic)
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.
Add multi-modality therapeutic radiation phantom, anthropomorphic to the RFQ basket or use the form below with quantity, specification and delivery location; the Network returns comparable quotes from verified suppliers in 2–5 working days.
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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.