Primo Passi
United Statesfrom the FDA registration address FDA establishment FEI 3034993050
- Devices
- 5
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3034993050
- Address
- 7524 Currency Dr., Orlando, FL, 32809
Frequently asked questions
How many devices does PRIMO PASSI have in the registry?
The registry currently lists 5 devices for PRIMO PASSI. Devices recorded under merged duplicate company entries are counted once.
Which registries list PRIMO PASSI's devices?
Among its 5 most recently registered devices, PRIMO PASSI has devices listed in FDA GUDID (5 devices).
What risk classes do PRIMO PASSI's devices fall under?
Among its 5 most recently registered devices, the classes recorded for PRIMO PASSI's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from PRIMO PASSI in the registry?
The most recently registered devices listed for PRIMO PASSI include Primo Passi JPD-FR300, Primo Passi XB-8732, Primo Passi 9229 and Primo Passi XB-8791.