Synapse medicine
FR-MF-000009699 · France · BORDEAUX
Synapse medicine is registered in the European database on medical devices as a manufacturer, with 12 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 6 |
|---|---|
| Class IIb | 6 |
Most frequent device types declared: Drug Safety System.
Among these devices, 12 are declared active.
Devices declared under this manufacturer
- Adverse events
- Dosage check
- Drug clinical alerts
- Drug interactions
- Drug safety system
- Geriatric guidelines
Catalogue references include Analyse clinique, Analyse de posologie, Drug Interactions, Drug Safety System, Drug clinical alerts, Effets indésirables.
European nomenclature codes declared: Z12040282, Z12040292.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 12 |
| 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. Synapse medicine was not found in either the U.S. or the Canadian register.