Soluscope SAS
FR-MF-000011763 · France · Aubagne
Soluscope SAS is registered in the European database on medical devices as a manufacturer, with 73 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 39 |
|---|---|
| Class IIa | 34 |
Most frequent device types declared: SL-TEE, SL-TEE-AT-ECL, SL-V1-AL-GTA, SL-V1-GTA, SL-V1-PA.
Among these devices, 25 are declared active.
Devices declared under this manufacturer
- DSC 8000
- MODULE ENDOSCOPIQUE EASYTOUCH
- SOLUSCOPE A
- SOLUSCOPE ECL-ENZYM. CLEAN. 2X5L + RFID
- SOLUSCOPE ECL-ENZYMATIC CLEANER 2X5L
- SOLUSCOPE P
- Soluscope™ D
- Soluscope™ GTA
- Soluscope™ PAA
- Soluscope™ Serie 1
- Soluscope™ Serie 4
- Soluscope™ A
Showing 12 of 73 declared devices.
Catalogue references include 1242282, 13382828X, 22067368T, 2295796GZ, 248444742, 311448555.
European nomenclature codes declared: V0799, D050101, Z12011314, D01010102, Z12011311, Z12011301.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 73 |
| 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 | 65 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | SOLUSCOPE |
North American profile: Canada only. Soluscope SAS holds a Canadian licence but was not found in the U.S. register.