EXAKTUS - Material de Reabilitação Oral, S.A.
PT-MF-000014249 · Portugal · Vila Nova de Gaia
EXAKTUS - Material de Reabilitação Oral, S.A. is registered in the European database on medical devices as a manufacturer, with 82 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 82 |
|---|
Most frequent device types declared: Conventional Analogue.
Devices declared under this manufacturer
- Compatible Analog - Biotech Kontact
- Compatible Analog - Branemark HE 3.5
- Compatible Analog - Branemark HE 4.1
- Compatible Analog - Branemark HE 5.0
- Compatible Analog - Conelog INT 3.3
- Compatible Analog - Klockner Vega 3.0
- Compatible Analog - MIS Seven 3.3
- Compatible Analog - Multi Unit M.U 4.8
- Compatible Analog - Neodent HE 3.5
- Compatible Analog - Nobel Active 3.0
- Compatible Digital Analog - Anthogyr Axiom 3.3/3.4/4/4.6/5.2
- Compatible Digital Analog - Camlog INT 4.3
Showing 12 of 82 declared devices.
Catalogue references include AD1100.1.2, AD1900.3.1, AD200.1.1, AD800.1.3, BRNK116, BRNK119.
European nomenclature codes declared: Q010299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 82 |
| Country of registration | Portugal |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 82 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. EXAKTUS - Material de Reabilitação Oral, S.A. was not found in either the U.S. or the Canadian register.