Pfrimmer-Viggo GmbH & Co.
Country not established
- Devices
- 1
What Pfrimmer-Viggo GmbH & Co. makes
Pfrimmer-Viggo GmbH & Co. manufactures the Tutoplast Dura, which is a processed human tissue graft used in surgical procedures.
This device is classified as Class II and is listed in the FDA 510(k) registry, with the company based in the US.
Catalogue
Tutoplast Dura Ref K910555
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pfrimmer-Viggo GmbH & Co. have in the registry?
The registry currently lists 1 device for Pfrimmer-Viggo GmbH & Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pfrimmer-Viggo GmbH & Co.'s devices?
Among its 1 most recently registered device, Pfrimmer-Viggo GmbH & Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Pfrimmer-Viggo GmbH & Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pfrimmer-Viggo GmbH & Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pfrimmer-Viggo GmbH & Co. in the registry?
The most recently registered devices listed for Pfrimmer-Viggo GmbH & Co. include TUTOPLAST DURA.