Laboratoire Aguettant
FR-MF-000000509 · France · LYON
Laboratoire Aguettant is registered in the European database on medical devices as a manufacturer, with 15 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 2 |
|---|---|
| Class IIa | 12 |
Among these devices, 11 are declared sterile.
Devices declared under this manufacturer
- BIDON EAU STERILE 5L
- BLUE MARKER AGUETTANT® DE
- BLUE MARKER AGUETTANT® EU
- DRUG SPRAYING CANNULAS
- ELISA Ricine eZYDIAG®
- MINIVERSOL® Sterile water
- MINIVERSOL® sterile sodium chloride 0.9%
- VERSOL® sterile sodium chloride 0.9% 1000mL
- VERSOL® sterile sodium chloride 0.9% 250 mL
- VERSOL® sterile sodium chloride 0.9% 500 mL
- VERSOL® sterile water 1000 mL
- VERSOL® sterile water 250 mL
Showing 12 of 15 declared devices.
Catalogue references include 600017, 600019, 600020, 600427, 600674, 64252.
European nomenclature codes declared: V0999, A13, V9099, Z12011385, Q02030299,Q030103,V0999, W0102090299,W01029099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 15 |
| 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 | 6 |
|---|---|
| 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. Laboratoire Aguettant was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
40393 | supplemented | 2028-08-07 |