LIFEAZ SAS
FR-MF-000009348 · France · Paris
LIFEAZ SAS is registered in the European database on medical devices as a manufacturer, with 30 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 15 |
|---|---|
| Class I | 15 |
Among these devices, 30 are declared active.
Devices declared under this manufacturer
- AED CLARK 2G DE
- AED CLARK 2G FR
- AED CLARK 2G IT
- AED CLARK 4G DE
- AED CLARK 4G DE PRO
- AED CLARK 4G DK
- AED CLARK 4G ES
- AED CLARK 4G FR
- AED CLARK 4G FR PRO
- AED CLARK 4G HU PRO
- AED CLARK 4G IT
- AED CLARK 4G IT PRO
Showing 12 of 30 declared devices.
Catalogue references include LFZ00473, LFZ00474, LFZ00475, LFZ00478, LFZ00495, LFZ00499.
European nomenclature codes declared: Z12030503.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 30 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 30 |
|---|---|
| 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. LIFEAZ SAS was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
G70 003159 0004 | amended | 2031-08-11 |
G15 003159 0007 | amended | 2030-05-11 |