Maquet GmbH and Co. KG
GermanyFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Maquet GmbH and Co. KG have in the registry?
The registry currently lists 1 device for Maquet GmbH and Co. KG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Maquet GmbH and Co. KG's devices?
Among its 1 most recently registered device, Maquet GmbH and Co. KG has devices listed in FDA 510(k) (1 device).
What risk classes do Maquet GmbH and Co. KG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Maquet GmbH and Co. KG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Maquet GmbH and Co. KG in the registry?
The most recently registered devices listed for Maquet GmbH and Co. KG include BORA UP 2080, BORA UP 2080 OP AND BORA UP 2080 MOUNTING.