IDCP BV
NL-MF-000000755 · Netherlands · Almere
IDCP BV is registered in the European database on medical devices as a manufacturer, with 23 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 23 |
|---|
Most frequent device types declared: Dino-Lite CapillaryScope, Dino-Lite DermaScope, Dino-Lite EarScope, Dino-Lite IriScope, Dino-Lite PodoScope.
Devices declared under this manufacturer
- Dino-Lite
- Dino-Lite CapillaryScope
- Dino-Lite DermaScope
- Dino-Lite EarScope
- Dino-Lite EarScope Basic Touch
- Dino-Lite PodoScope
- Dino-Lite TrichoScope
Showing 12 of 23 declared devices.
Catalogue references include MEDL3E, MEDL3H, MEDL4HM, MEDL4R, MEDL7HM, MEDLW4HM.
European nomenclature codes declared: Z12040118, Z12021009, Z12120199, Z12021007.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 23 |
| 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 | 23 |
|---|---|
| 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. IDCP BV was not found in either the U.S. or the Canadian register.