Dase Co.
Country not established
- Devices
- 1
What Dase Co. makes
Dase Co. manufactures a new support system designed to assist bedridden patients, providing stability and mobility assistance in clinical or home care settings.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. The portfolio is regulated in the United States.
Catalogue
New Support Sys. For Bedridden Patients Ref K821185
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dase Co. have in the registry?
The registry currently lists 1 device for Dase Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dase Co.'s devices?
Among its 1 most recently registered device, Dase Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Dase Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dase Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dase Co. in the registry?
The most recently registered devices listed for Dase Co. include NEW SUPPORT SYS. FOR BEDRIDDEN PATIENTS.