- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 18, 2026
4547327DGW003P33 references
4547327DGW003P3No device characteristics flagged
4202096CE014202096TD03Basic 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.
C04010201Coronary artery therapeutic guidewires, hydrophilic3 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 |
|---|---|---|---|---|---|
| ASAHI Miracle Neo 3 | ASAHI Miracle Neo 3 | AH14R012P | 04547327139830 | 1 | On the market |
| ASAHI Miracle Neo 3 | ASAHI Miracle Neo 3 | AH14R312P | 04547327139847 | 1 | On the market |
| ASAHI Miracle Neo 3 | ASAHI Miracle Neo 3 | AH14R212P | 04547327139854 | 1 | On the market |