EUDAMED device
LOGIQ Fortis
EUDAMED device 00195278835741 · GE Ultrasound Korea Ltd
Key facts
| Primary DI | 00195278835741 |
|---|---|
| Device name | LOGIQ Fortis |
| Reference or catalog number | LOGIQ Fortis R3 to R4 SW Upgrade / 5946725 |
| Model | LOGIQ Fortis |
| Manufacturer | GE Ultrasound Korea Ltd |
| Manufacturer SRN | KR-MF-000001860 |
| Risk class | Class IIa |
| EMDN code | Z11040101 |
| EMDN description | INTERNAL ULTRASOUND SCANNERS |
| Legislation | mdr |
| Implantable | No |
| Sterile | No |
| Single use | No |
| Status date | Mar 4, 2024 |
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: