Pharmia Oy
FI-MF-000001469 · Finland · Tuusula
Pharmia Oy is registered in the European database on medical devices as a manufacturer, with 65 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 65 |
|---|
Most frequent device types declared: 10 ml, 15 ml, 50 ml, LMED04, LMED04.1.
Devices declared under this manufacturer
- APTEEKKI Hoitava nenäsuihke, piparminttu
- ColdZinc sugtabletter 40 st
- LaktasDUO 80 kapslar
- Metode neseolje m/vitA
- Metode+ Nesespray 100% Sesamolje
- NASO Fresh seesamiöljy ratiopharm
- Nasolin A-vitamin Sitruuna-Mentoli
- Nasolin Kosteuttava nenäsuihke 20 ml
- No Zone
- Nozoil Aerozol do nosa
- Näsolja Apofri Nässpray
- Näsolja Punkt
Showing 12 of 65 declared devices.
Catalogue references include LADD01, LADD04, LEVO01.2, LEVO09, LORN97, LPHC03.
European nomenclature codes declared: Q030103, Q030199, G0401, Q0399.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 65 |
| Country of registration | Finland |
⚠️ 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 | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. Pharmia Oy was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
CR-03-1183-810-22 | supplemented | 2027-11-30 |