- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 31, 2026
B-087193271161971 reference
B-08719327116197CE 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.
W0105010118Chlamydia pneumoniae detection by na reagentsW0105010503Legionella detection by na reagentsW0105010803Mycoplasma / ureaplasma detection by na reagentsW0105011607Bordetella pertussis / parapertussis - na reagentsW0105040501Adenovirus - na reagentsW0105040502Enterovirus - na reagentsW0105040504Influenza & para influenza - na reagentsW0105040505Respiratory syncytial virus (rsv) - na reagentsW0105040517Human metapneumovirus - na reagentsW0105040518Bocavirus - na reagentsW0105040519—W0105040520Rhinovirus - 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 |
|---|---|---|---|---|---|
| RespiFinder® 2SMART | RespiFinder® 2SMART | PF2600-2S | 08719327116197 | 1 | On the market |