Data from EUDAMED, last updated Jul 30, 2026
42513158D-5613IVDLA2 references
42513158D-5613IVDLABasic 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.
W0106010301Down's syndromeW0106010302Edwards syndromeW0106010303Klinefelter syndromeW0106010304Pätau syndromeW0106010305Turner syndromeW0106010306Multiple detection of chromosomal disorders tests2 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 |
|---|---|---|---|---|---|
| XA AneuScore III | XA AneuScore III | D-5613-500-TC | 04251315813519 | 1 | On the market |
| XA AneuScore III | XA AneuScore III | D-5613-100-TC | 04251315813502 | 1 | On the market |