- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 31, 2026
4031881G11-01IsMJ9 references
4031881G11-01IsMJBasic 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.
A019001Blunt needles9 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 |
|---|---|---|---|---|---|
| KD-FINE | KD-FINE | 907979 | 24031881907973 | 1 | On the market |
| KD-FINE | KD-FINE | 917145 | 24031881917149 | 1 | On the market |
| KD-FINE | KD-FINE | 907962 | 24031881907966 | 1 | On the market |
| KD-FINE BLUNT | KD-FINE BLUNT | 909300A | 54031881909305 | 1 | On the market |
| KD-FINE BLUNT | KD-FINE BLUNT | 910597 | 24031881910591 | 1 | On the market |
| KD-FINE BLUNT | KD-FINE BLUNT | 909294 | 24031881909298 | 1 | On the market |
| KD-FINE BLUNT | KD-FINE BLUNT | 910603A | 54031881910608 | 1 | On the market |
| KD-FINE BLUNT | KD-FINE BLUNT | 920299 | 24031881920293 | 1 | On the market |
| KD-FINE BLUNT | KD-FINE BLUNT | 920282 | 24031881920286 | 1 | On the market |