- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jun 17, 2026
924010SD10170GG3 references
924010SD10170GGBasic 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 →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.
W0105010899Mycoplasma / ureaplasma reagents - other3 references
| Product | Trade name | Reference / catalog number | UDI-DI code | Quantity | Status |
|---|---|---|---|---|---|
| Allplex™ MG & AziR Assay | Allplex™ MG & AziR Assay | SD10170X | 08809240101704 | 1 | On the market |
| Allplex™ MG & AziR Assay | Allplex™ MG & AziR Assay | SD10169Y | 08809240101698 | 1 | On the market |
| Allplex™ MG & AziR Assay | Allplex™ MG & AziR Assay | SD10319Z | 08809240103197 | 1 | On the market |