Philips France
Active in EUDAMEDFrancefrom SRN EUDAMED FDA SRN FR-MF-000038954 FEI 3033558564
- Devices
- 2
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
Cardiologs Platform Ref 2.4.X
Regimes: CE MDR Registry: EUDAMEDGUDID
Company details
- EUDAMED SRN
- FR-MF-000038954
- FDA FEI number
- 3033558564
- DUNS number
- 280036084
- EU VAT number
- FR72811847243
- EUDAMED status
- Active
- EUDAMED registered name
- Philips France
- Registered address
- 100, Rue Réaumur, 75002, Paris, France
- [email protected]
- PRRC contact
- Tahnee Mehta
Frequently asked questions
How many devices does PHILIPS FRANCE have in the registry?
The registry currently lists 2 devices for PHILIPS FRANCE. Devices recorded under merged duplicate company entries are counted once.
Which registries list PHILIPS FRANCE's devices?
Among its 2 most recently registered devices, PHILIPS FRANCE has devices listed in EUDAMED (1 device) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do PHILIPS FRANCE's devices fall under?
Among its 2 most recently registered devices, the classes recorded for PHILIPS FRANCE's devices are Class IIa and Class II. Each device page shows its own class and authorisation.
What are the newest devices from PHILIPS FRANCE in the registry?
The most recently registered devices listed for PHILIPS FRANCE include Cardiologs Platform 2.5.x and Cardiologs Platform.