Deron B.V.
NL-MF-000006051 · Netherlands · Gendt
Deron B.V. is registered in the European database on medical devices as a manufacturer, with 35 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 35 |
|---|
Most frequent device types declared: FullCare Twin HRC AD matras incl. hoes inco blauw 3zr , Papillon Twin HR AD matras incl. hoes inco blauw 3zr , AventoPore Twin HRC matras incl. hoes inco blauw 3zr , Kindermatras incl. hoes inco blauw 3zr, Zorgmatras koudschuim hoes inco blauw 3zr.
No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 35 |
| Country of registration | Netherlands |
⚠️ Absence here is not proof of absence from the market. A manufacturer may reach the United States through a distributor registered under its own name, or under a corporate name we could not match. We publish what we measured, not what we inferred.