Synopsys (Northern Europe) Ltd
GB-MF-000002376 · United Kingdom · Exeter
Synopsys (Northern Europe) Ltd is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 8 |
|---|
Most frequent device types declared: P-2019.09, Q-2020.03, Q-2020.06, R-2020.09, R-2021.03.
Among these devices, 8 are declared active, 1 with a measuring function.
Authorised representative in the Union: Synopsys International Ltd..
Devices declared under this manufacturer
- Simpleware Medical
- Simpleware ScanIP Medical
- Synopsys Simpleware ScanIP™ O-2018.12
- Synopsys Simpleware™ ScanIP
- Synopsys Simpleware™ ScanIP P-2019.09
Catalogue references include O-2018.12, P-2019.09, Q-2020.03, Q-2020.06, R-2020.09, R-2021.03.
European nomenclature codes declared: Z110603.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 8 |
| Country of registration | United Kingdom |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 8 |
|---|---|
| Found in the U.S. device database | 8 |
| Share | 100.0 % |
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. Synopsys (Northern Europe) Ltd was not found in either the U.S. or the Canadian register.