International safety notice
Aplicación StentBoost Live (referencia: 459801781661) usada con el sistema Philips Azurion
Spain / AEMPS · ESP · Feb 22, 2022
Key facts
| Title | Aplicación StentBoost Live (referencia: 459801781661) usada con el sistema Philips Azurion |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Aplicación StentBoost Live (referencia: 459801781661) usada con el sistema Philips Azurion |
| Manufacturer | Philips Medical Systems Nederland BV, Países Bajos |
| Models | 2022-086, 28050, 76806, 28022, 459801781661, 91.822.52.89, FCO72200503, 2021-IGT-BST-033 |
| Event type | Safety Notice |
| Date | Feb 22, 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