Data from EUDAMED, last updated Jul 31, 2026
890209590030FX5 references
890209590030FXNo 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.
A010401Arteriovenous fistula needles5 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 |
|---|---|---|---|---|---|
| AV Fistula Needle with/without safety features | AV Fistula Needle with/without safety features | 95059 | 08902095950593 | 1 | On the market |
| AV Fistula Needle with/without safety features | AV Fistula Needle with/without safety features | 95061 | 08902095950616 | 1 | On the market |
| AV Fistula Needle with/without safety features | AV Fistula Needle with/without safety features | 95058 | 08902095950586 | 1 | On the market |
| AV Fistula Needle with/without safety features | AV Fistula Needle with/without safety features | 95057 | 08902095950579 | 1 | On the market |
| AV Fistula Needle with/without safety features | AV Fistula Needle with/without safety features | 95060 | 08902095950609 | 1 | On the market |