Heraeus Medical GmbH Technology
GermanyFDA applicant, unverified
- Devices
- 1
What Heraeus Medical GmbH Technology makes
Heraeus Medical GmbH Technology manufactures the PALAMED, a medical device designed for surgical applications, including the preparation and handling of biological tissues during procedures.
The PALAMED is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Palamed Ref K030904
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Heraeus Medical GmbH Technology have in the registry?
The registry currently lists 1 device for Heraeus Medical GmbH Technology. Devices recorded under merged duplicate company entries are counted once.
Which registries list Heraeus Medical GmbH Technology's devices?
Among its 1 most recently registered device, Heraeus Medical GmbH Technology has devices listed in FDA 510(k) (1 device).
What risk classes do Heraeus Medical GmbH Technology's devices fall under?
Among its 1 most recently registered device, the classes recorded for Heraeus Medical GmbH Technology's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Heraeus Medical GmbH Technology in the registry?
The most recently registered devices listed for Heraeus Medical GmbH Technology include PALAMED.