MED2B Ltd.
Country not established FDA FEI 3035708926
- Devices
- 5
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3035708926
- DUNS number
- 313487375
- Address
- Lochweg 2A, Kitzingen Bavaria
Frequently asked questions
How many devices does MED2B LTD. have in the registry?
The registry currently lists 5 devices for MED2B LTD.. Devices recorded under merged duplicate company entries are counted once.
Which registries list MED2B LTD.'s devices?
Among its 5 most recently registered devices, MED2B LTD. has devices listed in FDA GUDID (5 devices).
What risk classes do MED2B LTD.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for MED2B LTD.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from MED2B LTD. in the registry?
The most recently registered devices listed for MED2B LTD. include Grace Medical 10-105-235, Grace Medical 10-105-238, Grace Medical 10-105-237 and Grace Medical 10-105-236.