Oy Finnsusp Ab
FI-MF-000011137 · Finland · Lieto
Oy Finnsusp Ab is registered in the European database on medical devices as a manufacturer, with 14 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 13 |
|---|---|
| Class IIa | 1 |
Most frequent device types declared: F0001, F0002, F0004, F0007, F0009.
Among these devices, 14 are declared sterile.
Devices declared under this manufacturer
- Biopex BioSoak
- Piiloset BioDrop
- Piiloset BioDrop MD
- Piiloset BioDrop MD PLUS
- Piiloset BioDrop MD SPRAY
- Piiloset BioTwin
- Piiloset CL Daily Cleaner
- Piiloset O2
- Piiloset OneStep
- Piiloset SAL Suolaliuos
- Puro Suoja
- Puro Vita
Showing 12 of 14 declared devices.
Catalogue references include F0001, F0002, F0004, F0007, F0009, F0010.
European nomenclature codes declared: Q02030206, Q02030204.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 14 |
| Country of registration | Finland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | OY FINNSUSP AB |
What it holds in Canada
| Licences on record | 3 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 3 |
| First licensed | 2017-10-19 |
Licence types: Single Device (3).
Licensed under: PIILOSET BIODROP MD COMFORT EYE DROPS, PIILOSET BIODROP MD PLUS INTENSIVE MOISTURIZER, PIILOSET BIODROP MD SPRAY.
North American profile: Canada only. Oy Finnsusp Ab holds a Canadian licence but was not found in the U.S. register.