Dörr Kampen B.V.
NL-MF-000000113 · Netherlands · Kampen
Dörr Kampen B.V. is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 9 |
|---|
Most frequent device types declared: Dörr Nova 1000, Dörr Nova 2000, Dörr Nova 4000, Dörr Nova Clean, Dörr scopenvoorreiniger.
Devices declared under this manufacturer
- Dörr ManoFlexibilo
- Dörr Nova 1000
- Dörr Nova 2000
- Dörr Nova 4000
- Dörr Nova Clean
- Dörr Nova Combi
- Dörr Nova Sonic
- Dörr scopenvoorreiniger
Catalogue references include 1020, 2020, 4020, 5014, 6018, 80.200.
European nomenclature codes declared: V0799, V0804, Z12011301, Z12011301,Z12011302, Z12011311, Z12011302.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 9 |
| 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 | 9 |
|---|---|
| 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. Dörr Kampen B.V. was not found in either the U.S. or the Canadian register.