AAZ PRODUCTIONS LE MATERIEL BIOMEDICAL
FR-MF-000015889 · France · BOULOGNE-BILLANCOURT
AAZ PRODUCTIONS LE MATERIEL BIOMEDICAL is registered in the European database on medical devices as a manufacturer, with 18 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: TR-THC-001.
Devices declared under this manufacturer
- CANNABIS ALL IN
- COV-GRIP
- COVID-VIRO
- CRP ALL IN
- CYSTI'TEST
- TROD'ANGINE
- TROD'ANGINE+
- TROD'DENGUE
- TetaQuick
- autotest VIH® 2nd GENERATION
Showing 12 of 18 declared devices.
Catalogue references include AS-VIH-001, AS-VIH-009, AS-VIH-011, TR-ANG-008, TR-ANG-009, TR-COV-006.
European nomenclature codes declared: W0105090302, W0105040619, W0101060204, W0105090103, W0105090106, W0105040611.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 18 |
| 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 | 18 |
|---|---|
| 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. AAZ PRODUCTIONS LE MATERIEL BIOMEDICAL was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
40540 | issued | 2031-06-02 |
40028 | supplemented | 2029-10-08 |