Laboratoire Medix
FranceFDA applicant, unverified
- Devices
- 1
What Laboratoire Medix makes
Laboratoire Medix manufactures the BIAFINE device, a medical product classified under class U.
The BIAFINE device is regulated through the FDA 510(k) pathway and is listed in the fda_510k registry; the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Biafine Ref K943910
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Laboratoire Medix have in the registry?
The registry currently lists 1 device for Laboratoire Medix. Devices recorded under merged duplicate company entries are counted once.
Which registries list Laboratoire Medix's devices?
Among its 1 most recently registered device, Laboratoire Medix has devices listed in FDA 510(k) (1 device).
What are the newest devices from Laboratoire Medix in the registry?
The most recently registered devices listed for Laboratoire Medix include BIAFINE.