International safety notice
Interruptor del pedal alámbrico e inalámbrico de los sistemas Allura Xper, Allura Centron, Azurion y MultiDiagnost-Eleva. Ver nos de referencia y modelos afectados en el apéndice B de la nota de aviso de la empresa.
Spain / AEMPS · ESP · Dec 21, 2023
Key facts
| Title | Interruptor del pedal alámbrico e inalámbrico de los sistemas Allura Xper, Allura Centron, Azurion y MultiDiagnost-Eleva. Ver nos de referencia y modelos afectados en el apéndice B de la nota de aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Interruptor del pedal alámbrico e inalámbrico de los sistemas Allura Xper, Allura Centron, Azurion y MultiDiagnost-Eleva. Ver nos de referencia y modelos afectados en el apéndice B de la nota de aviso de la empresa. |
| Manufacturer | Philips Medical Systems Nederland BV, Holanda. |
| Models | 459800076004, 459800772212, 452270000383, 459800772203, 452270000152, 97048, 459800772193, 2023-416.LA, 459800772201, 459800772191, 459800076021, 459800076023 and 33 more |
| Event type | Safety Notice |
| Date | Dec 21, 2023 |
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