International safety notice
Sistemas gammacámara BrightView, BrightView X y BrightView XCT. Ver números de modelos afectados en la nota de aviso de la empresa.
Spain / AEMPS · ESP · Jan 30, 2024
Key facts
| Title | Sistemas gammacámara BrightView, BrightView X y BrightView XCT. Ver números de modelos afectados en la nota de aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistemas gammacámara BrightView, BrightView X y BrightView XCT. Ver números de modelos afectados en la nota de aviso de la empresa. |
| Manufacturer | Philips Medical Systems Nederland B.V. Países Bajos. |
| Models | 2024-058, 453560279801, 453560279791, 453560462131453560749161, 453560749161, 882480, 28050, 91.822.52.89, 2170-3001A, 2170-3002A, 453560279781453560279791453560279811453560279801, 2023-PD-CTAMI-011 and 14 more |
| Event type | Safety Notice |
| Date | Jan 30, 2024 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers 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