Data from EUDAMED, last updated Jul 31, 2026
3664977EMDNZ12020701P82 references
3664977EMDNZ12020701P8Basic 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.
Z12020701Cystoscopes2 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 |
|---|---|---|---|---|---|
| Cystoflex™ Reverse Deflection | Cystoflex™ Reverse Deflection | 11010012 | 03664977000066 | 1 | On the market |
| Cystoflex™ Standard Deflection | Cystoflex™ Standard Deflection | 11010011 | 03664977000059 | 1 | On the market |