- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 31, 2026
8437016942GVS-MTH-MRE3 references
8437016942GVS-MTH-MREBasic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →SRN
An SRN is the unique EUDAMED identifier assigned to a manufacturer, authorised representative or importer when it registers as an actor.
View in glossary →European Medical Device Nomenclature — the EU product classifications carried across this device family's references.
W0106010116Other thrombophilia mutations (proc, pros1, mthfr, serpinc1, sepine1, f11, f12, f13, other f2/f5)3 references
| Product | Trade name | Reference / catalog number | Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary → | Quantity | Status |
|---|---|---|---|---|---|
| Genvinset® MTHFR multiplex 24 test | Genvinset® MTHFR multiplex 24 test | GVS-MTH-M-24 | 08437016942826 | 1 | On the market |
| Genvinset® MTHFR multiplex 48 test | Genvinset® MTHFR multiplex 48 test | GVS-MTH-M-48 | 08437016942833 | 1 | On the market |
| Genvinset® MTHFR multiplex 96 test | Genvinset® MTHFR multiplex 96 test | GVS-MTH-M-96 | 08437016942840 | 1 | On the market |