anthogyr
FR-MF-000000602 · France · Sallanches
anthogyr is registered in the European database on medical devices as a manufacturer, with 1 725 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIb | 954 |
|---|---|
| Class IIa | 771 |
Most frequent device types declared: Axiom TL Implant, Unitary Non-Sterile Abutment/Base/Coping (Titanium), Implant bed preparation instrument, Axiom BL Implant, Plural Non-Sterile Abutment/Base/Coping (Titanium).
Among these devices, 588 are declared sterile, 954 implantable, 40 reusable, 14 active.
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 | Registered with FDA |
|---|---|
| Matched entry | ANTHOGYR (FR) · FDA 8020776 |
| Devices in EUDAMED | 1 725 |
| Country of registration | France |