Germitec
Country not established FDA establishment FEI 3030303856
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Chronos® Ref DEN230067
Regimes: De Novo Registry: De Novo
Company details
- FDA FEI number
- 3030303856
- Address
- 19 rue Vauban, Bordeaux Nouvelle-Aquitaine
FDA establishments
- Germitec US
Frequently asked questions
How many devices does GERMITEC have in the registry?
The registry currently lists 1 device for GERMITEC. Devices recorded under merged duplicate company entries are counted once.
Which registries list GERMITEC's devices?
Among its 1 most recently registered device, GERMITEC has devices listed in FDA 510(k) (1 device).
What risk classes do GERMITEC's devices fall under?
Among its 1 most recently registered device, the classes recorded for GERMITEC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from GERMITEC in the registry?
The most recently registered devices listed for GERMITEC include Chronos®.
Which FDA establishments are linked to GERMITEC?
1 FDA establishment is linked to GERMITEC in the registry; they are listed on the company page.