EBG MedAustron GmbH
Austria AT-MF-000002630 Last updated 21 Oct 2026
- Devices
- 2
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
About
Ion therapy enables individualized high-precision, local cancer treatment. Only in a few locations worldwide can this be done with both protons and carbon ions, as with MedAustron.
What EBG MedAustron GmbH makes
EBG MedAustron GmbH develops and operates advanced ion therapy systems for cancer treatment, including the MATEO and MAPTA devices. These systems deliver high-precision proton and carbon ion radiotherapy, enabling targeted therapy for localized tumors. The technology is designed to minimize exposure to surrounding healthy tissue while optimizing treatment outcomes for complex cases.
The company’s devices fall under EU Class IIb classification and are registered in the EU’s eudamed database. MedAustron is headquartered in Austria, where its systems are authorized for clinical use under applicable European Union medical device regulations.
Frequently asked questions
What types of medical devices does EBG MedAustron GmbH manufacture or operate?
EBG MedAustron GmbH specializes in advanced ion therapy systems for cancer treatment. Specifically, they develop and operate devices like MATEO and MAPTA, which deliver high-precision proton and carbon ion radiotherapy. These technologies are designed to target tumors with localized precision while minimizing exposure to surrounding healthy tissue, making them suitable for complex or localized cancer cases.
Where is EBG MedAustron GmbH based, and where are its devices authorized for use?
EBG MedAustron GmbH is headquartered in Austria. Their ion therapy systems, including MATEO and MAPTA, are authorized for clinical use in the European Union under applicable medical device regulations. The company’s devices are registered in the EU’s eudamed database, which tracks authorized medical devices within the region.
How are EBG MedAustron GmbH’s devices classified under EU medical device regulations?
EBG MedAustron GmbH’s devices, such as MATEO and MAPTA, fall under EU Class IIb classification. This classification is assigned based on the risk associated with the device—Class IIb devices are considered higher-risk than Class I or IIa but not as high as Class III. The classification influences regulatory requirements, including clinical evaluation and conformity assessment procedures.
Are EBG MedAustron GmbH’s devices listed in any public regulatory registries?
Yes, EBG MedAustron GmbH’s devices are registered in the eudamed database, which is the official EU registry for medical devices. This database is maintained by the European Commission and serves as a transparent resource for stakeholders—including healthcare professionals, regulators, and patients—to verify the authorization status of devices marketed in the EU.
Information
- Country
- Austria
- Address
- 5, Marie Curie-Straße, Wiener Neustadt, Austria
- Website
- www.medaustron.at
- [email protected]
- Phone
- +43 2622 26100
- PRRC contact
- Katharina Kraßer
- EUDAMED SRN
- AT-MF-000002630