Textielbewerking VDM
NL-MF-000005879 · Netherlands · Numansdorp
Textielbewerking VDM is registered in the European database on medical devices as a manufacturer, with 11 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 11 |
|---|
Most frequent device types declared: Glijlaken & Rollslide, Traagschuim anti-decubitus zitkussens.
Devices declared under this manufacturer
- Glijlaken 100x150
- Glijlaken 140x200
- Glijlaken 90x110
- Glijlaken maatwerk
- Rollslide 90x110
- Rollslide maatwerk
- Traagschuim zitkussen met IC hoes - 45x45x6,5 cm
- Traagschuim zitkussen met IC hoes – 42x46x6,5 cm
- Traagschuim zitkussen met IC hoes – 48x50x6,5 cm
- Traagschuim zitkussen met IC hoes– maatwerk
- Traagschuim zitkussen met uitsparing en IC hoes - 42 x 42 x 8 cm
Catalogue references include 3060150, 3060151, 3060153, 3060159, 3600001, 3600002.
European nomenclature codes declared: V80, V08030102.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 11 |
| 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 | 11 |
|---|---|
| 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. Textielbewerking VDM was not found in either the U.S. or the Canadian register.