Semperit Technische Produkte Gesellchaft M.B.H.
AustriaFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Semperit Technische Produkte Gesellchaft M.B.H. have in the registry?
The registry currently lists 1 device for Semperit Technische Produkte Gesellchaft M.B.H.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Semperit Technische Produkte Gesellchaft M.B.H.'s devices?
Among its 1 most recently registered device, Semperit Technische Produkte Gesellchaft M.B.H. has devices listed in FDA 510(k) (1 device).
What risk classes do Semperit Technische Produkte Gesellchaft M.B.H.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Semperit Technische Produkte Gesellchaft M.B.H.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Semperit Technische Produkte Gesellchaft M.B.H. in the registry?
The most recently registered devices listed for Semperit Technische Produkte Gesellchaft M.B.H. include Sterile Powder-Free Synthetic Rubber Surgeon’s Glove with Low Dermatitis Potential.