Plasti - Ape - S.p.A.
Active in EUDAMEDItalyfrom SRN EUDAMED FDA SRN IT-MF-000027167
- Devices
- 1
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA establishment
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Monodose Dry Powder Inhalation Device Ref 0CNA0A115AA.BB._
Regimes: CE MDR Registry: EUDAMED
Company details
- EUDAMED SRN
- IT-MF-000027167
- EU VAT number
- 10728530154
- EUDAMED status
- Active
- EUDAMED registered name
- PLASTI - APE - S.P.A.
- EUDAMED abbreviated name
- Plastiape
- Registered address
- 8, Via Primo Maggio, 23875, Osnago, Italy
- [email protected]
- PRRC contact
- Cristina Tremolada
FDA establishments
- PLASTIAPE S.p.A Osnago Lecco · IT FEI 3003805036
Frequently asked questions
How many devices does PLASTI - APE - S.P.A. have in the registry?
The registry currently lists 1 device for PLASTI - APE - S.P.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list PLASTI - APE - S.P.A.'s devices?
Among its 1 most recently registered device, PLASTI - APE - S.P.A. has devices listed in EUDAMED (1 device).
What risk classes do PLASTI - APE - S.P.A.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for PLASTI - APE - S.P.A.'s devices are Class IIa. Each device page shows its own class and authorisation.
What are the newest devices from PLASTI - APE - S.P.A. in the registry?
The most recently registered devices listed for PLASTI - APE - S.P.A. include Monodose Dry Powder Inhalation Device.
Which FDA establishments are linked to PLASTI - APE - S.P.A.?
1 FDA establishment is linked to PLASTI - APE - S.P.A. in the registry; they are listed on the company page.