EUDAMED device
[ARVIS - Instruments] Hex Driver
EUDAMED device 00810180350709 · Kico Knee Innovation Company Pty Ltd
Key facts
| Primary DI | 00810180350709 |
|---|---|
| Device name | [ARVIS - Instruments] Hex Driver |
| Reference or catalog number | IN-10800 |
| Manufacturer | Kico Knee Innovation Company Pty Ltd |
| Manufacturer SRN | AU-MF-000011477 |
| Risk class | Class I |
| EMDN code | L26 |
| EMDN description | SURGICAL SCREWDRIVERS, REUSABLE |
| Legislation | mdr |
| Implantable | No |
| Sterile | No |
| Single use | No |
| Status date | Sep 2, 2025 |
At a glance
- Yes Matching FDA GUDID record
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About EUDAMED devices
EUDAMED is the European Union's database of medical devices registered under the MDR and IVDR, including UDI-DIs, risk classes and EMDN nomenclature codes.
Source: European Commission, European Database on Medical Devices (EUDAMED) · Source date: