International safety notice
Sistemas Artis. Ver nombres de producto y números de modelo afectados en el documento adjunto 1 de la nota de aviso de la empresa.
Spain / AEMPS · ESP · Apr 2, 2024
Key facts
| Title | Sistemas Artis. Ver nombres de producto y números de modelo afectados en el documento adjunto 1 de la nota de aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistemas Artis. Ver nombres de producto y números de modelo afectados en el documento adjunto 1 de la nota de aviso de la empresa. |
| Manufacturer | Siemens Healthcare GmbH, Alemania. |
| Models | 2022-257, 4056869012667, 4056869010106, 4056869010045, 4056869010014, 4056869012711, AX005, 4056869009988, 4056869010083, 4056869012674, 2022-257.LA, 4056869009971 and 20 more |
| Event type | Safety Notice |
| Date | Apr 2, 2024 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models 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