Interster International B.V.
NL-MF-000002615 · Netherlands · Wormerveer
Interster International B.V. is registered in the European database on medical devices as a manufacturer, with 145 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 145 |
|---|
Devices declared under this manufacturer
- Crêpe Sensitive White / Blue 100x100cm
- Diana Cap
- Meatex HD Blue / Interwrap 340 Green 100x100cm
- Meatex HD Blue / Regular Green 120x140cm
- Meatex HD Blue / Secu-Wrap Regular Green 150x180cm ECO
- Meatex Regular Blue / Green 100x100cm LOS
- Meatex Regular Blue / Green 140x140cm
- Meatex Xtreme Blue / Interwrap 340 Green 100x100cm
- Meatex Xtreme Blue / Regular Green 140x140cm
- Secu-wrap All In One 140x180cm ECO
- Secu-wrap Standard Blue 140x140cm
- Twinwrap 3 140x140cm
Showing 12 of 145 declared devices.
Catalogue references include 3FDOP384904, 3FDOP387810, 3FITL377804, 3FITL383820, 3FITL384830, 3FITL387816.
European nomenclature codes declared: S010302, T0207.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 145 |
| 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 | 145 |
|---|---|
| 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. Interster International B.V. was not found in either the U.S. or the Canadian register.