EUDAMED device
DUROLANE®
EUDAMED device 00816986020181 · Bioventus LLC
Key facts
| Primary DI | 00816986020181 |
|---|---|
| Trade name | DUROLANE® |
| Device name | DUROLANE® hyaluronic acid, stabilized single injection (3mL) |
| Reference or catalog number | 1082010 |
| Model | 1082010 |
| Manufacturer | Bioventus LLC |
| Manufacturer SRN | US-MF-000008452 |
| Risk class | Class III |
| EMDN code | P900402 |
| EMDN description | RESORBABLE FILLING AND RECONSTRUCTION DEVICES |
| Legislation | mdd |
| Implantable | Yes |
| Sterile | Yes |
| Single use | Yes |
| Status date | Oct 25, 2024 |
At a glance
- No 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: