Carpenter Engineered Foams Oy
Active in EUDAMEDFinlandfrom SRN EUDAMED FDA SRN FI-MF-000040986
- Devices
- 69
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA establishment
Catalogue
Search and filter all 69 devicesShowing 1-50 of 69
Company details
- EUDAMED SRN
- FI-MF-000040986
- EU VAT number
- FI18328477
- EUDAMED status
- Active
- EUDAMED registered name
- Carpenter Engineered Foams Oy
- Registered address
- 2, Nevantie, 45200, Kouvola, Finland
- [email protected]
- Phone
- +358405537843
- PRRC contact
- Merja-Liisa Vuori
FDA establishments
- Carpenter Engineered Foams SAS FR
Frequently asked questions
How many devices does Carpenter Engineered Foams Oy have in the registry?
The registry currently lists 69 devices for Carpenter Engineered Foams Oy. Devices recorded under merged duplicate company entries are counted once.
Which registries list Carpenter Engineered Foams Oy's devices?
Among its 50 most recently registered devices, Carpenter Engineered Foams Oy has devices listed in EUDAMED (50 devices).
What risk classes do Carpenter Engineered Foams Oy's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Carpenter Engineered Foams Oy's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Carpenter Engineered Foams Oy in the registry?
The most recently registered devices listed for Carpenter Engineered Foams Oy include EVAK. PREMIUM-50 97x200x13 V65+R50, MDR EVAK. PREMIUM-50 78x220x13 V65+R50, EVAK. PREMIUM-50 88x200x13 V65+R50 and EVAK. PREMIUM-50 78x200x13 V65+R50.
Which FDA establishments are linked to Carpenter Engineered Foams Oy?
1 FDA establishment is linked to Carpenter Engineered Foams Oy in the registry; they are listed on the company page.