SurgVision GmbH
Active in EUDAMEDGermanyfrom SRN EUDAMED FDA SRN DE-MF-000006163 FEI 3026934906
- Devices
- 2
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
Catalogue
- Regimes: 510(k) Registry: 510(k)
Explorer Air Ii Ref 8002
Regimes: CE MDR 510(k) Registry: EUDAMEDGUDID
Company details
- EUDAMED SRN
- DE-MF-000006163
- FDA FEI number
- 3026934906
- DUNS number
- 343632898
- EU VAT number
- DE 337761485
- EUDAMED status
- Active
- EUDAMED registered name
- SurgVision GmbH
- EUDAMED abbreviated name
- SVN
- Registered address
- 70, Kistlerhofstr.,, 81379, Muenchen, Germany
- [email protected]
- Phone
- +31645767502
- PRRC contact
- Nils Beyer
Frequently asked questions
How many devices does SurgVision GmbH have in the registry?
The registry currently lists 2 devices for SurgVision GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list SurgVision GmbH's devices?
Among its 2 most recently registered devices, SurgVision GmbH has devices listed in EUDAMED (1 device), FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do SurgVision GmbH's devices fall under?
Among its 2 most recently registered devices, the classes recorded for SurgVision GmbH's devices are Class IIa and Class II. Each device page shows its own class and authorisation.
What are the newest devices from SurgVision GmbH in the registry?
The most recently registered devices listed for SurgVision GmbH include EXPLORER AIR® II (8001, 8002, 8003); EXPLORER AIR® Sterile Drape (8004) and EXPLORER AIR II.