- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 31, 2026
697360079019K42 references
697360079019K4TD-CE-TB-IGRA-06-02-CPR-A1Basic 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.
W0105010704Tb-igra (interferon-gamma-release assay)2 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 |
|---|---|---|---|---|---|
| INNODX TB-IGRA CMIA | INNODX TB-IGRA CMIA | KR-TB-IGRA-01020C | 06973600799824 | 1 | On the market |
| INNODX TB-IGRA CMIA | INNODX TB-IGRA CMIA | KR-TB-IGRA-01050W | 06973600799831 | 1 | On the market |