PreTect AS
Active in EUDAMEDNorwayfrom SRN EUDAMED FDA SRN NO-MF-000051817 FEI 3017889386
- Devices
- 5
- 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
PreTect X Ref 111002
Regimes: CE IVDR Registry: EUDAMEDPreTect TM Stock Solution Ref 400201
Regimes: CE IVDR Registry: EUDAMEDPreTect TM Ref 400251
Regimes: CE IVDR Registry: EUDAMEDPreTect X Ref 111001
Regimes: CE IVDR Registry: EUDAMEDPreTect TM Ref 400101
Regimes: CE IVDR Registry: EUDAMED
Company details
- EUDAMED SRN
- NO-MF-000051817
- FDA FEI number
- 3017889386
- EU VAT number
- NO980001288MVA
- EUDAMED status
- Active
- EUDAMED registered name
- PreTect AS
- EUDAMED abbreviated name
- PreTect
- Registered address
- 8, USTADHAGAN, 3490, Klokkarstua, Norway
- Website
- www.pretect.no/
- [email protected]
- Phone
- +4732798800
- PRRC contact
- Bente Marie Falang
Frequently asked questions
How many devices does PreTect AS have in the registry?
The registry currently lists 5 devices for PreTect AS. Devices recorded under merged duplicate company entries are counted once.
Which registries list PreTect AS's devices?
Among its 5 most recently registered devices, PreTect AS has devices listed in EUDAMED (5 devices).
What risk classes do PreTect AS's devices fall under?
Among its 5 most recently registered devices, the classes recorded for PreTect AS's devices are IVDR Class A. Each device page shows its own class and authorisation.
What are the newest devices from PreTect AS in the registry?
The most recently registered devices listed for PreTect AS include PreTect X, PreTect TM Stock Solution and PreTect TM.