Formafoam BV
NL-MF-000006056 · Netherlands · Born
Formafoam BV is registered in the European database on medical devices as a manufacturer, with 27 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 27 |
|---|
Catalogue references include S045690, S045691, S045697, S045777, S050179, S051331.
European nomenclature codes declared: V080702, V0880, V08030102, V080302.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 27 |
| Country of registration | Netherlands |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 27 |
|---|---|
| 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. Formafoam BV was not found in either the U.S. or the Canadian register.