International safety notice
Sistema de Resonancia Magnética (RM) Philips.
Spain / AEMPS · ESP · Apr 17, 2024
Key facts
| Title | Sistema de Resonancia Magnética (RM) Philips. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistema de Resonancia Magnética (RM) Philips. |
| Manufacturer | Philips Healthcare, Países Bajos. |
| Models | 782113, 781102, 781358, 782138, 28050, 781344, 781315, 781356, 781343, 781171, 782119, 78107 and 73 more |
| Event type | Safety Notice |
| Date | Apr 17, 2024 |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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