Madshus A/S
NorwayFDA applicant, unverified
- Devices
- 1
What Madshus A/S makes
Madshus A/S manufactures the MOLIFT, which is a Class I medical device.
The company is based in the US and the MOLIFT device is listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Molift Ref K851844
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Madshus A/S have in the registry?
The registry currently lists 1 device for Madshus A/S. Devices recorded under merged duplicate company entries are counted once.
Which registries list Madshus A/S's devices?
Among its 1 most recently registered device, Madshus A/S has devices listed in FDA 510(k) (1 device).
What risk classes do Madshus A/S's devices fall under?
Among its 1 most recently registered device, the classes recorded for Madshus A/S's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Madshus A/S in the registry?
The most recently registered devices listed for Madshus A/S include MOLIFT.