International safety notice
Sistema de Resonancia Magnética Prodiva 1.5T, modelo 781069
Spain / AEMPS · ESP · Aug 24, 2021
Key facts
| Title | Sistema de Resonancia Magnética Prodiva 1.5T, modelo 781069 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistema de Resonancia Magnética Prodiva 1.5T, modelo 781069 |
| Manufacturer | Philips Healthcare (Suzhou) Co., Ltd., China |
| Models | 82298, 82480, “FCO78100533, 2021-472, 781069, 5.416, 28022, 71517, A-28017143, 82428, 2021-PD-MR-001, 91.822.52.89 and 3 more |
| Event type | Safety Notice |
| Date | Aug 24, 2021 |
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