Idevax BV
BE-MF-000028217 · Belgium · Wijnegem
Idevax BV is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 6 |
|---|
Most frequent device types declared: VAX-ID® 2200.
Devices declared under this manufacturer
- VAX-ID® 2200 27G sterile
- VAX-ID® 2200 27G to be sterilized
- VAX-ID® 2200 30G sterile
- VAX-ID® 2200 30G to be sterilized
- VAX-ID® 2200 32G sterile
- VAX-ID® 2200 32G to be sterilized
Catalogue references include D00035, D00036, D00037, D00046, D00047, D00048.
European nomenclature codes declared: A018002.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| Country of registration | Belgium |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 6 |
|---|---|
| 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. Idevax BV was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
ECM25MDR008 | issued | 2030-03-31 |