Hans-Juergen Huchel
Country not established
- Devices
- 1
What Hans-Juergen Huchel makes
Hans-Juergen Huchel manufactures the HUCHEL BODYLINER, a medical device designed for use in orthopedic and spinal procedures to provide structural support during surgical interventions.
The HUCHEL BODYLINER is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The manufacturer operates from the United States.
Catalogue
Huchel Bodyliner Ref K873576
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hans-Juergen Huchel have in the registry?
The registry currently lists 1 device for Hans-Juergen Huchel. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hans-Juergen Huchel's devices?
Among its 1 most recently registered device, Hans-Juergen Huchel has devices listed in FDA 510(k) (1 device).
What risk classes do Hans-Juergen Huchel's devices fall under?
Among its 1 most recently registered device, the classes recorded for Hans-Juergen Huchel's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hans-Juergen Huchel in the registry?
The most recently registered devices listed for Hans-Juergen Huchel include HUCHEL BODYLINER.