International safety notice
Philips StentBoost Live R2.0 rakendus - hõive ei peatu automaatselt, röntgenpilte ei töödelda
Estonia / EMDDB · EST · Feb 1, 2022
Key facts
| Title | Philips StentBoost Live R2.0 rakendus - hõive ei peatu automaatselt, röntgenpilte ei töödelda |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Philips StentBoost Live R2.0 rakendus |
| Manufacturer | PHILIPS STENTBOOST LIVE R20 RAKENDUS |
| Models | v6tab, t66delda, FCO72200503, V6ite, h6ivatakse, k6rgeima, Ettev6tte, m6istmist, m6jutatud, n6uetekohaselt, v6tke, k6igile and 1 more |
| Date | Feb 1, 2022 |
| Regulator page | terviseamet.ee |
At a glance
- No Recall
- No 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