Hennig Enterprises Europe SRL
Country not established
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Go Medical Patient Controlled Analgesia Devices Ref K020421
Regimes: 510(k) Registry: 510(k)V Set Ref K020424
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hennig Enterprises Europe Srl have in the registry?
The registry currently lists 2 devices for Hennig Enterprises Europe Srl. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hennig Enterprises Europe Srl's devices?
Among its 2 most recently registered devices, Hennig Enterprises Europe Srl has devices listed in FDA 510(k) (2 devices).
What risk classes do Hennig Enterprises Europe Srl's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Hennig Enterprises Europe Srl's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hennig Enterprises Europe Srl in the registry?
The most recently registered devices listed for Hennig Enterprises Europe Srl include GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES and V SET.