Carpenter Engineered Foams Oy
FI-MF-000040986 · Finland · Kouvola
Carpenter Engineered Foams Oy is registered in the European database on medical devices as a manufacturer, with 58 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIa | 58 |
|---|
Devices declared under this manufacturer
- FYSICON EVAKUOINTI PREMIUM-50S 88x200x17 cm
- FYSICON MINIMAX 117*200*13 CM
- Fysicon Basic 75*190*12 cm
- Fysicon Basic 90*200*12 cm
- Fysicon Evak. MiniMAX 75x200x13 cm
- Fysicon Evakuointi MiniMAX 80x200x15 cm
- Fysicon Premium jatkopala 90x20x13 cm
- Fysicon jatkopala 80x20x13 cm
- Fysicon jatkopala 90x20x13 cm
- Fysicon korotustyyny 40*40*7 cm
- Fysicon korotustyyny 40*45*5 cm
- Fysicon lonkkatyyny 40*40*10 cm ½
Showing 12 of 58 declared devices.
Catalogue references include 3501006959, 3501007518, 3501008162, 3501009732, 3501010083, 3501010086.
European nomenclature codes declared: V080702, V080399, V0899.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | Carpenter ENGINEERED FOAMS GERMANY GMBH (DE) · FDA 3009335681 |
| Devices in EUDAMED | 58 |
| Country of registration | Finland |
⚠️ A similar name exists; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 58 |
|---|---|
| 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.