- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Aug 13, 2026
4063106ASTGWXPX3 references
4063106ASTGWXPXNo 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 →European Medical Device Nomenclature — the EU product classifications carried across this device family's references.
K0180Endotherapy devices - other accessories3 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 |
|---|---|---|---|---|---|
| aerstent GWA | aerstent GWA | 901-35-180 | 14063106101098 | 1 | On the market |
| aerstent GWA | aerstent GWA | 912-35-180 | 14063106101111 | 1 | On the market |
| aixstent GWG | aixstent GWG | 904-35-260 | 14063106101104 | 1 | On the market |