EUDAMED device
Actiwatch Spectrum PRO-Recertified
EUDAMED device 00606959409835 · Respironics Inc.
Key facts
| Primary DI | 00606959409835 |
|---|---|
| Trade name | Actiwatch Spectrum PRO-Recertified |
| Device name | Actiwatch Spectrum Pro and Actiwatch Spe |
| Reference or catalog number | U1099351 |
| Manufacturer | Respironics Inc. |
| Manufacturer SRN | US-MF-000002301 |
| Risk class | Class IIa |
| EMDN code | Z12040117 |
| EMDN description | METABOLIC AND PHYSICAL ACTIVITY HOLTER SYSTEMS |
| Legislation | mdd |
| Implantable | No |
| Sterile | No |
| Single use | No |
| Status date | Dec 31, 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: