- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 31, 2026
B-087193271161281 reference
B-08719327116128CE 737648Basic 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.
W0104080207Mycoplasma / ureaplasma - (incl. combined id-ast)W0105010117Chlamydia trachomatis detection by na reagentsW0105010305Syphilis detection by na reagentsW0105010803Mycoplasma / ureaplasma detection by na reagentsW0105040311Hsv - na reagentsW0105070501Stis / stds (c.trachomatis, n.gonorrhoeae ,m.genitalium, t.vaginalis, ureaplasma spp….) combination - multiplex na reagents1 reference
| 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 |
|---|---|---|---|---|---|
| STD-Finder® 2SMART | STD-Finder® 2SMART | PF3200-2S | 08719327116128 | 1 | On the market |