International safety notice
Interruptor de pedal alámbrico de los sistemas Allura Xper, Allura Centron, Azurion y MultiDiagnost Eleva. Ver números de referencia afectados en el apéndice B de las notas de aviso de la empresa.
Spain / AEMPS · ESP · Oct 5, 2023
Key facts
| Title | Interruptor de pedal alámbrico de los sistemas Allura Xper, Allura Centron, Azurion y MultiDiagnost Eleva. Ver números de referencia afectados en el apéndice B de las notas de aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Interruptor de pedal alámbrico de los sistemas Allura Xper, Allura Centron, Azurion y MultiDiagnost Eleva. Ver números de referencia afectados en el apéndice B de las notas de aviso de la empresa. |
| Manufacturer | Philips Medical Systems Nederland BV, Países Bajos. |
| Models | 452270000151, 459800076002, 97373, 452270000141, AD7XT, 452270000381, 28022, 459800772201, 459800772191, 459800076024, 452270000154, 459800076023 and 36 more |
| Event type | Safety Notice |
| Date | Oct 5, 2023 |
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