International safety notice
Philips Medical Systems Xper Flex Cardio Devices - meeldetuletus, seade ei pruugi naasta tavapärasesse töörežiimi
Estonia / EMDDB · EST · Sep 1, 2023
Key facts
| Title | Philips Medical Systems Xper Flex Cardio Devices - meeldetuletus, seade ei pruugi naasta tavapärasesse töörežiimi |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Philips Medical Systems Xper Flex Cardio Devices |
| Manufacturer | PHILIPS MEDICAL SYSTEMS XPER FLEX CARDIO DEVICES |
| Models | 02-JAA-2021, FC2020, 2023-CC-HPM-022, FC2010, tulem1 |
| Date | Sep 1, 2023 |
| 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