Dirinco B.V.
NL-MF-000002150 · Netherlands · Oss
Dirinco B.V. 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 IIb | 6 |
|---|
Among these devices, 6 are declared sterile.
Devices declared under this manufacturer
- Citra-Lock™ Catheter lock solution 30%
- Citra-Lock™ Catheter lock solution 4%
- Citra-Lock™ Catheter lock solution 46.7%
Catalogue references include 24060201, 24060202, 24060203.
European nomenclature codes declared: C0199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| 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 | 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. Dirinco B.V. was not found in either the U.S. or the Canadian register.