EUDAMED device
23ga ACTU8 Myopic Tewari (T2) Forceps
EUDAMED device 00810123481163 · Vortex Surgical Inc
Key facts
| Primary DI | 00810123481163 |
|---|---|
| Device name | 23ga ACTU8 Myopic Tewari (T2) Forceps |
| Reference or catalog number | VS0742.23-35 |
| Manufacturer | Vortex Surgical Inc |
| Manufacturer SRN | US-MF-000022888 |
| Risk class | Class IIa |
| EMDN code | Q020599 |
| EMDN description | RETINAL DETACHMENT DEVICES - OTHER |
| Legislation | mdd |
| Implantable | No |
| Sterile | Yes |
| Single use | Yes |
| Status date | Dec 19, 2022 |
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: