International safety notice
Sistemas de resonancia magnética (RM) de GE Healthcare: SIGNA, Discovery, Optima y Brivo Ver modelos y versiones de software afectadas en la nota de aviso de la empresa
Spain / AEMPS · ESP · Jul 5, 2024
Key facts
| Title | Sistemas de resonancia magnética (RM) de GE Healthcare: SIGNA, Discovery, Optima y Brivo Ver modelos y versiones de software afectadas en la nota de aviso de la empresa |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistemas de resonancia magnética (RM) de GE Healthcare: SIGNA, Discovery, Optima y Brivo Ver modelos y versiones de software afectadas en la nota de aviso de la empresa |
| Manufacturer | GE Medical Systems LLC, Estados Unidos GE Hangwei Medical Systems CO.Ltd GE Healthcare (Tianjin) Company Limited GE Healthcare Japan Corporation. |
| Models | DV29.0, DV27.1, MR750, 00840682135283, 00195278372307, SV25.5, MR380, MR355, 00840682144445, RX29.0, 00840682146302, MP24.0 and 112 more |
| Event type | Safety Notice |
| Date | Jul 5, 2024 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1