Dumco B.V.
NL-MF-000050760 · Netherlands · Sprang-Capelle
Dumco B.V. is registered in the European database on medical devices as a manufacturer, with 62 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 62 |
|---|
Most frequent device types declared: Women’s model: Size 36–42 Men’s model: Size 40–48, Women’s model: Size 36–42 Men’s model: Size 40–48.
Devices declared under this manufacturer
- Medisole Achilles Men size 40
- Medisole Achilles Men size 43
- Medisole Achilles Women size 36
- Medisole Achilles Women size 41
- Medisole Diabetes & Rheumatism Men size 40
- Medisole Forefoot Men size 45
- Medisole Forefoot Women size 40
- Medisole Forefoot Women size 42
- Medisole Heel Spur Men size 40
- Medisole Heel Spur Men size 43
- Medisole Heel Spur Men size 45
- Medisole Heel Spur Men size 46
Showing 12 of 62 declared devices.
Catalogue references include 53102040, 53102145, 53103036, 53103140, 53103143, 53104037.
European nomenclature codes declared: Y061203.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 62 |
| 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 | 62 |
|---|---|
| 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. Dumco B.V. was not found in either the U.S. or the Canadian register.