EUDAMED device
Actiwatch 2 Device Recertified
EUDAMED device 00606959409781 · Respironics Inc.
Key facts
| Primary DI | 00606959409781 |
|---|---|
| Trade name | Actiwatch 2 Device Recertified |
| Reference or catalog number | U1048090 |
| Model | Actiwatch 2 and Actiwatch Spectrum |
| Manufacturer | Respironics Inc. |
| Manufacturer SRN | US-MF-000002301 |
| Risk class | Class IIa |
| EMDN code | Z12062599 |
| EMDN description | KINEMATIC MOTION CAPTURE ANALYSIS SYSTEMS - OTHER |
| Legislation | mdd |
| Implantable | No |
| Sterile | No |
| Single use | No |
| Status date | Jul 16, 2025 |
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: