- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 31, 2026
52980048NIPTTJ2 references
52980048NIPTTJBasic 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.
W0106010101Cystic fibrosisW0106010109Sickle cell anemiaW0106010110Tay sachs diseaseW0106010111ThalassaemiaW0106010199Monogenetic disorders tests - otherW0106010301Down's syndromeW0106010302Edwards syndromeW0106010304Pätau syndromeW0106010305Turner syndromeW0106010306Multiple detection of chromosomal disorders testsW0106010399Chromosomal disorders tests - other2 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 |
|---|---|---|---|---|---|
| VERACITY Advance | VERACITY Advance | EV101-00-2096 | 05298004820013 | 1 | On the market |
| VERACITY Premium | VERACITY Premium | EV102-00-2096 | 05298004820044 | 1 | On the market |