Data from EUDAMED, last updated Jul 31, 2026
B-089041183882221 reference
B-08904118388222TAXCO/001SiBi/001TFLEX/MR/001279275-2018-CE-IND-NA-PS279276-2018-CE-IND-NA-PSCTRI/2019/11/022088ISRCTN39751665CTRI/2019/05/019298CTRI/2019/05/019297Basic 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.
P070402010301Coronary drug eluting stents (des) with polymers1 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 |
|---|---|---|---|---|---|
| Supraflex Cruz | Supraflex Cruz | FGTZ250008 | 08904118388222 | 1 | On the market |