- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jun 21, 2026
924010HP10372FX2 references
924010HP10372FXBasic 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.
W0105041004Full genotyping high-risk + low-risk hpv - na reagents2 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 |
|---|---|---|---|---|---|
| Allplex™ HPV28 Detection | Allplex™ HPV28 Detection | HP10372X | 08809240103722 | 1 | On the market |
| Allplex™ HPV28 Detection | Allplex™ HPV28 Detection | HP10373Z | 08809240103739 | 1 | On the market |