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Applied Medical Europe

Also registered as Applied Medical Europe B.V.

Netherlandsfrom SRN FDA establishment FEI 3009763019

Devices
462
Registrations
FDA
FDA recalls
0

Catalogue462

Newest first, page 1 of 10

Showing 1-50 of 462

Company details

FDA FEI number
3009763019
Address
Wiekenweg 21, Amersfoort Utrecht

Frequently asked questions

How many devices does Applied Medical Europe have in the registry?

The registry currently lists 462 devices for Applied Medical Europe. Devices recorded under merged duplicate company entries are counted once.

Which registries list Applied Medical Europe's devices?

Among its 50 most recently registered devices, Applied Medical Europe has devices listed in EUDAMED (50 devices).

What risk classes do Applied Medical Europe's devices fall under?

Among its 50 most recently registered devices, the classes recorded for Applied Medical Europe's devices are Class IIa and Class IIb. Each device page shows its own class and authorisation.

What are the newest devices from Applied Medical Europe in the registry?

The most recently registered devices listed for Applied Medical Europe include CP005, AME STANDARD KIT, GK705 and GK1034.

Generated automatically from registry data and not verified by a human reviewer.

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.