Van der Mark Anti Decubitus Systemen
NL-MF-000005763 · Netherlands · Numansdorp
Van der Mark Anti Decubitus Systemen is registered in the European database on medical devices as a manufacturer, with 20 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 20 |
|---|
Most frequent device types declared: Bedhekbeschermer, Luchtwisseldruk matras.
Devices declared under this manufacturer
- Bedhekbeschermer 100 cm - met instopstrook
- Bedhekbeschermer 100cm t.b.v. Sentida bed van 200cm (geschikt voor dee
- Bedhekbeschermer 110cm t.b.v. voeteneinde Sentida bed van 210cm (gesch
- Bedhekbeschermer 198cm, 5 sluitingen
- Bedhekbeschermer 198cm, 5 sluitingen - met instopstrook
- Bedhekbeschermer 208cm, 5 sluitingen
- Bedhekbeschermer hoofdeinde links/rechts te gebruiken t.b.v. FMB Formi
- Bedhekbeschermer hoofdeinde t.b.v. FMB First bed | 92x26
- Bedhekbeschermer voeteneinde links/rechts te gebruiken t.b.v. FMB Form
- Bedhekbeschermer voeteneinde t.b.v. FMB First bed 220cm | 117x26 | lin
- High flow 100 Heavy Duty
- High flow 120 Heavy Duty
Showing 12 of 20 declared devices.
Catalogue references include 1120875, 136.17011, 136.17021, 136.17030, 136.17034, 136.17035.
European nomenclature codes declared: V08068001, V080701.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 20 |
| 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 | 20 |
|---|---|
| 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. Van der Mark Anti Decubitus Systemen was not found in either the U.S. or the Canadian register.