Greiner Bio-One Vacuette North America
Country not established
- Devices
- 5
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Vacuette Trace Elements Tubes Ref K023971
Regimes: 510(k) Registry: 510(k)Safety Infusion Set Ref K080235
Regimes: 510(k) Registry: 510(k)Vacuette Evacuated Blood Collection Tubes Ref K011699
Regimes: 510(k) Registry: 510(k)Vacuette Quickshield Safety Tube Holder Ref K033478
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Greiner Bio-One Vacuette North America have in the registry?
The registry currently lists 5 devices for Greiner Bio-One Vacuette North America. Devices recorded under merged duplicate company entries are counted once.
Which registries list Greiner Bio-One Vacuette North America's devices?
Among its 5 most recently registered devices, Greiner Bio-One Vacuette North America has devices listed in FDA 510(k) (5 devices).
What risk classes do Greiner Bio-One Vacuette North America's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Greiner Bio-One Vacuette North America's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Greiner Bio-One Vacuette North America in the registry?
The most recently registered devices listed for Greiner Bio-One Vacuette North America include VACUETTE EDTA K3 EVACUATED BLOOD COLLECTION TUBES, VACUETTE TRACE ELEMENTS TUBES, SAFETY INFUSION SET and VACUETTE EVACUATED BLOOD COLLECTION TUBES.