Streekziekenhuis Koningin Beatrix
NL-MF-000000427 · Netherlands · Winterswijk
Streekziekenhuis Koningin Beatrix is registered in the European database on medical devices as a manufacturer, with 35 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- HbA1c, Frozen Whole Blood set
- HbA1c, Lyophilised hemolysate Level 1
- HbA1c, Lyophilised hemolysate Level 2
- HbA1c, Lyophilised hemolysate Level 3
- HbA1c, Lyophilised hemolysate Level High
- HbA1c, Lyophilised hemolysate Level Low
- HbA1c, ingevroren volbloed Level 2
- Virtamin B1/B6, Level 3
- Vitamin B1/B6, Level 2
- Vitamin B1/B6, Level 6
- Vitamin B1/B6, Level Low
- Vitamine B1/B6, set 6x Medium
Showing 12 of 35 declared devices.
Catalogue references include HBA-01.1_011, HBA-01.3_011, HBA-04.3, VTB-01.1, VTB-01.2, VTB-02.61.
European nomenclature codes declared: W0101050205,W0101050302, W0101050101,W0101050301, W0101050299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 35 |
| 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 | 33 |
|---|---|
| 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. Streekziekenhuis Koningin Beatrix was not found in either the U.S. or the Canadian register.