EUDAMED device
Acutip
EUDAMED device 00816722022806 · Cutera, Inc.
Key facts
| Primary DI | 00816722022806 |
|---|---|
| Trade name | Acutip |
| Device name | xeo+ |
| Reference or catalog number | 7003139 |
| Manufacturer | Cutera, Inc. |
| Manufacturer SRN | US-MF-000010456 |
| Risk class | Class IIb |
| EMDN code | Z12011019 |
| EMDN description | MULTI-PLATFORM LASER |
| Legislation | mdr |
| Implantable | No |
| Sterile | No |
| Single use | No |
| Status date | Mar 19, 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: