Schell B.V.
NetherlandsFDA applicant, unverified
- Devices
- 1
What Schell B.V. makes
Schell B.V. manufactures the SCHELL C.A.P.P. BED, models NRS. 1268 and 1269, which are designed for patient positioning and support in clinical settings, likely for therapeutic or rehabilitation purposes.
The SCHELL C.A.P.P. BED is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Schell C.A.P.P. Bed Model Nrs. 1268 + 1269 Ref K871368
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Schell B.V. have in the registry?
The registry currently lists 1 device for Schell B.V.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Schell B.V.'s devices?
Among its 1 most recently registered device, Schell B.V. has devices listed in FDA 510(k) (1 device).
What risk classes do Schell B.V.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Schell B.V.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Schell B.V. in the registry?
The most recently registered devices listed for Schell B.V. include SCHELL C.A.P.P. BED MODEL NRS. 1268 + 1269.