SIA Laboveritas
LV-MF-000018225 · Latvia · Riga
SIA Laboveritas is registered in the European database on medical devices as a manufacturer, with 11 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: 0011, 0012, 0014, 0016, 0017.
Devices declared under this manufacturer
- Express Genetics DNA
- ExtraMag 1000
- Laboveritas
- Magnetite
- VeriLab Express DNA
- VeriLab ExtraMag 500
- VeriLab UMag
- Verilab GMag
- Verilab GVTM
- Verilab RVTM
- Verilab USorb
Catalogue references include 070102, LVE-0011, LVE-0012, LVE-0014, LVE-0020, LVT-0016.
European nomenclature codes declared: W0105900101, W0104010203, W0299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 11 |
| Country of registration | Latvia |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 11 |
|---|---|
| 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. SIA Laboveritas was not found in either the U.S. or the Canadian register.