- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 31, 2026
69502033TEBY10 references
69502033TEBYNo device characteristics flagged
Basic 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.
U03010202Ureteral dilators10 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 |
|---|---|---|---|---|---|
| IVX-TE-2161 | — | IVX-TE-2161 | 06950203360088 | 1 | On the market |
| IVX-TE-2141 | — | IVX-TE-2141 | 06950203360071 | 1 | On the market |
| IVX-TE-1181 | — | IVX-TE-1181 | 06950203360101 | 1 | On the market |
| IVX-TE-2091 | — | IVX-TE-2091 | 06950203360033 | 1 | On the market |
| IVX-TE-2181 | — | IVX-TE-2181 | 06950203360095 | 1 | On the market |
| IVX-TE-2081 | — | IVX-TE-2081 | 06950203360026 | 1 | On the market |
| IVX-TE-2121 | — | IVX-TE-2121 | 06950203360064 | 1 | On the market |
| IVX-TE-2111 | — | IVX-TE-2111 | 06950203360057 | 1 | On the market |
| IVX-TE-2061 | — | IVX-TE-2061 | 06950203360019 | 1 | On the market |
| IVX-TE-2101 | — | IVX-TE-2101 | 06950203360040 | 1 | On the market |