Imtmedical AG
SwitzerlandFDA applicant, unverified
- Devices
- 6
What Imtmedical AG makes
Imtmedical AG manufactures the bellavista 1000 and Bellavista, which are medical imaging devices designed for vascular and interventional procedures, including angiography and fluoroscopy.
These products are classified as Class II devices under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
bellavista 1000 Ref K163127
Regimes: 510(k) Registry: 510(k)Bellavista Ref K183364
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 483243700
- [email protected]
- Phone
- +1(833)327-3284
Frequently asked questions
How many devices does Imtmedical AG have in the registry?
The registry currently lists 6 devices for Imtmedical AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Imtmedical AG's devices?
Among its 6 most recently registered devices, Imtmedical AG has devices listed in FDA 510(k) (2 devices) and FDA GUDID (4 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Imtmedical AG's devices fall under?
Among its 6 most recently registered devices, the classes recorded for Imtmedical AG's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Imtmedical AG in the registry?
The most recently registered devices listed for Imtmedical AG include EVair M1230847, EVair M1230849, bellavista 1000 and imtmedical 302.578.000.