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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 IIa771
Class IIb954

Most frequent device types declared: Axiom BL Implant, Axiom TL Implant, Dalbo analog, Implant bed preparation instrument, Laboratory AxIN base.

Among these devices, 588 are declared sterile, 954 implantable, 40 reusable, 14 active.

Devices declared under this manufacturer

Showing 12 of 1 725 declared devices.

Catalogue references include AT40100, AX156-01B-ET, AXIN156-02-L, GTA46G50L, MIOFC_NOT, OPAF032.

European nomenclature codes declared: P010299, P01020101, L159099, Q010299, Q010207, V0599.

United States market access

FDA establishment registerRegistered with FDA
Matched entryANTHOGYR (FR) · FDA 8020776
Devices in EUDAMED1 725
Country of registrationFrance

Device-level evidence

Devices with a numeric GTIN1 725
Found in the U.S. device database718
Share41.6 %

Canadian market access

Health Canada licence listingLicensed in Canada
Matched entryANTHOGYR

What it holds in Canada

Licences on record8
Currently active0
Class 2 devices6
Class 3 devices2
First licensed2012-03-14

Licence types: System (5), Device Family (3).

Licensed under: CONTRE-ANGLES ET PIECES A MAIN DE CHIRURGIE, CONTRE-ANGLES D'ENDODONTIE, PERIOTOMES (EXOSAFE), SAFE RELAX - DEPOSE - COURONNES ET BRIDGES AUT, CONTRE-ANGLES D'IMPLANTOLOGIE, OSTEOTOMES (OSTEOSAFE).

North American profile: Both markets. anthogyr is registered in both the United States and Canada.

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