VANDERWILT techniques bv
NL-MF-000011827 · Netherlands · Boxtel
VANDERWILT techniques bv is registered in the European database on medical devices as a manufacturer, with 143 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 143 |
|---|
Devices declared under this manufacturer
- FOR-MED.nl
- for-med.nl
Showing 12 of 143 declared devices.
Catalogue references include 1117.100, 749.400, 886.008, 886.060, 886.074, 886.132.
European nomenclature codes declared: V0880.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 143 |
| 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 | 143 |
|---|---|
| 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. VANDERWILT techniques bv was not found in either the U.S. or the Canadian register.