Merck Biomaterial GmbH
GermanyFDA applicant, unverified
- Devices
- 1
What Merck Biomaterial GmbH makes
Merck Biomaterial GmbH produces PALAMED BONE CEMENT, a medical device used in orthopedic procedures.
The device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the US.
Catalogue
Palamed Bone Cement Ref K010586
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Merck Biomaterial GmbH have in the registry?
The registry currently lists 1 device for Merck Biomaterial GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Merck Biomaterial GmbH's devices?
Among its 1 most recently registered device, Merck Biomaterial GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Merck Biomaterial GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Merck Biomaterial GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Merck Biomaterial GmbH in the registry?
The most recently registered devices listed for Merck Biomaterial GmbH include PALAMED BONE CEMENT.