E.A.M Benelux B.v
Country not established FDA establishment FEI 3042175944
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
QF10 Ref K261470
510(k) 510(k)
Company details
- FDA FEI number
- 3042175944
- Address
- Korenbloemweg 79, ALMERE Flevoland
Frequently asked questions
How many devices does E.A.M BENELUX B.V have in the registry?
The registry currently lists 1 device for E.A.M BENELUX B.V. Devices recorded under merged duplicate company entries are counted once.
Which registries list E.A.M BENELUX B.V's devices?
Among its 1 most recently registered device, E.A.M BENELUX B.V has devices listed in FDA 510(k) (1 device).
What risk classes do E.A.M BENELUX B.V's devices fall under?
Among its 1 most recently registered device, the classes recorded for E.A.M BENELUX B.V's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from E.A.M BENELUX B.V in the registry?
The most recently registered devices listed for E.A.M BENELUX B.V include QF10.