SYMATESE DEVICE
FR-MF-000020651 · France · Irigny
SYMATESE DEVICE is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 9 |
|---|
Most frequent device types declared: 0202, 0231, Set de transfert.
Among these devices, 6 are declared sterile.
Devices declared under this manufacturer
- CLIP INJECT
- OPHTAJECT
- Rectal Cannula
- Set de transfert
Catalogue references include 0202NA, 0202NC, 0202PA, 0222NA, 0231NL, 0231NM.
European nomenclature codes declared: Q0299, V0299, A0704.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | SYMATESE DEVICE (FR) · FDA 3011224555 |
| Devices in EUDAMED | 9 |
| Country of registration | France |
Device-level evidence
| Devices with a numeric GTIN | 9 |
|---|---|
| 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: United States only. SYMATESE DEVICE is registered in the United States but was not found in the Canadian register.