Oy Fluorplast Ab
FI-MF-000015708 · Finland · Petolahti
Oy Fluorplast Ab is registered in the European database on medical devices as a manufacturer, with 129 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 129 |
|---|
Among these devices, 75 are declared sterile.
Catalogue references include 9055, 9321A, 9327, 9361, BRCD-XL-STE, SIL010030.
European nomenclature codes declared: R03010204, A060102, A06010103, T030199, A06010199, A0399.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 129 |
| 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 | 129 |
|---|---|
| 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. Oy Fluorplast Ab was not found in either the U.S. or the Canadian register.