Eurotape B.V.
NL-MF-000001956 · Netherlands · Soest
Eurotape B.V. is registered in the European database on medical devices as a manufacturer, with 494 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 494 |
|---|
Most frequent device types declared: Construction Tape CDT, Inserts, LCP, OP-Film, OP-Strips.
Devices declared under this manufacturer
- Med/PE175H+
- Med/TUR E10 LF
- OP-Film S232
- OP-Film S235
- OP-Film S238
- OP-Film S272
- OP-Film S275
- OP-Film S279
- OP-Film S282
- OP-Tape S070
- OP-Tape S073
- SteriShape DC-PEW
Showing 12 of 494 declared devices.
Catalogue references include S070.030100.0F, S073.125400.2F, S073.270200.2F, S272.2524-20, S272.25250-2XM, S272.4555-20.
European nomenclature codes declared: V9099, T02010101.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 494 |
| 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 | 494 |
|---|---|
| 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. Eurotape B.V. was not found in either the U.S. or the Canadian register.