WellMed BV
NL-MF-000023115 · Netherlands · Arnhem
WellMed BV is registered in the European database on medical devices as a manufacturer, with 242 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- Antibody diluent
- BrightDiluent
- BrightVision
- BrightVision Ultimate
- BrightVision Ultmate (plus)
- BrigthDiluent
- BrigthVision
- CryoCompound
- Draco
- HIER buffer Tris/EDTA
- HIER buffer citrate
- Imsolmount
Showing 12 of 242 declared devices.
Catalogue references include C-T50AP, DPVB110AP, DPVR500AP, O1000AP, UBVO999HRP, YAD09-125.
European nomenclature codes declared: W01029003, W01030704, W01030706.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 242 |
| 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 | 242 |
|---|---|
| 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. WellMed BV was not found in either the U.S. or the Canadian register.