International safety notice
Sistema de información cardiológica MUSE X R1 de versiones SP2 y superiores con la opción de edición web. Ver UDI’s en la nota de aviso de la empresa.
Spain / AEMPS · ESP · May 20, 2022
Key facts
| Title | Sistema de información cardiológica MUSE X R1 de versiones SP2 y superiores con la opción de edición web. Ver UDI’s en la nota de aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistema de información cardiológica MUSE X R1 de versiones SP2 y superiores con la opción de edición web. Ver UDI’s en la nota de aviso de la empresa. |
| Manufacturer | GE Medical Systems Information Technologies, Inc., Estados Unidos |
| Models | DCAR.30102, MUSENXSP3, 3101011-040, 46117, 30102-2, 53188, 91.822.52.89, 28022, 3101010-401, 79529, MUSENXSP2, 2022-239 and 4 more |
| Event type | Safety Notice |
| Date | May 20, 2022 |
At a glance
- No Recall
- Yes Field safety notice
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