Mannesmann Demag Corp.
Country not established
- Devices
- 1
What Mannesmann Demag Corp. makes
Mannesmann Demag Corp. manufactures powered patient manipulating devices, including the PK-AC model, designed for assisting in patient positioning and handling within clinical settings.
The company’s portfolio is regulated under FDA Class II devices, with products listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Pk-Ac Powered Patient Manupulating Device Ref K854058
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mannesmann Demag Corp. have in the registry?
The registry currently lists 1 device for Mannesmann Demag Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mannesmann Demag Corp.'s devices?
Among its 1 most recently registered device, Mannesmann Demag Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Mannesmann Demag Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mannesmann Demag Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mannesmann Demag Corp. in the registry?
The most recently registered devices listed for Mannesmann Demag Corp. include PK-AC POWERED PATIENT MANUPULATING DEVICE.