# Durolane®

> Active: European Union. Medical device record on deviCERTS, compiled from public registries.

- Canonical page: <https://devicerts.com/devices/durolane-r-1082010>
- Manufacturer: [Bioventus LLC](https://devicerts.com/manufacturers/bioventus-llc) (United States)
- Name in the registry: DUROLANE®
- Device class: Class III (EU MDD)
- EMDN: P900402 RESORBABLE FILLING AND RECONSTRUCTION DEVICES

## Registrations and authorizations

- **EUDAMED** · CE/MDD · European Union · Basic UDI-DI B-00816986020181 · UDI-DI 00816986020181 · registered 2024-10-25 · status: Active

## Recalls

No recall on record.

## EU market availability

- Austria
- Belgium
- Bulgaria
- Croatia
- Cyprus
- Czechia
- Denmark
- Estonia
- Finland
- France
- Germany
- Greece
- Hungary
- Iceland
- Ireland
- Italy
- Latvia
- Liechtenstein
- Lithuania
- Luxembourg
- Malta
- Netherlands
- Northern Ireland
- Norway
- Poland
- Portugal
- Romania
- Slovakia
- Slovenia
- Spain
- Sweden
- Türkiye

## Identity

- Device name: DUROLANE® hyaluronic acid, stabilized single injection (3mL) [EUDAMED]
- Model / reference: 1082010 [EUDAMED]

## Identifiers

- Primary DI / UDI-DI: 00816986020181 [EUDAMED]
- Basic UDI-DI: B-00816986020181 [EUDAMED]
- EMDN code: P900402 [EUDAMED]

## Classification

- Device class: Class III [EUDAMED]
- EU registration type: Legacy device (under a directive) [EUDAMED]
- EU market of registration: Netherlands [EUDAMED]

## Properties

- Supplied sterile: Yes [EUDAMED]
- Implantable: Yes [EUDAMED]
- Sterilise before use: No [EUDAMED]
- Reusable: No [EUDAMED]
- Contains latex: No [EUDAMED]
- Reprocessed single-use device: No [EUDAMED]
- Incorporates a substance derived from human blood or plasma: No [EUDAMED]
- Contains human tissues or cells: No [EUDAMED]
- Contains animal tissues or cells: No [EUDAMED]
- Administering medicine: No [EUDAMED]
- Measuring function: No [EUDAMED]
- Incorporates a medicinal substance: No [EUDAMED]

## Source and citation

- Cite as: Durolane®, Bioventus LLC. deviCERTS medical device catalogue. https://devicerts.com/devices/durolane-r-1082010 (data as of 2026-11-15).
- Data sources: [EUDAMED](https://ec.europa.eu/tools/eudamed)
- Registry records last synced: 2026-10-23
- Statuses computed as of: 2026-11-15
- JSON: <https://devicerts.com/devices/durolane-r-1082010.json>
- Licence: [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/). The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.
- Attribution: DevicErts, https://devicerts.com/devices/durolane-r-1082010
- Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails.