International safety notice
Philips Xper Flex Cardio patsiendi jälgimissüsteemid - reaalaja EKG ja rõhukõvera anomaalia, SpO2, vererõhu vale näit
Estonia / EMDDB · EST · Jan 1, 2019
Key facts
| Title | Philips Xper Flex Cardio patsiendi jälgimissüsteemid - reaalaja EKG ja rõhukõvera anomaalia, SpO2, vererõhu vale näit |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Philips Xper Flex Cardio patsiendi jälgimissüsteemid |
| Manufacturer | PHILIPS XPER FLEX CARDIO PATSIENDI JÄLGIMISSÜSTEEMID |
| Models | 453564483331, 453564669081, 453564241911, FC2010, rakendamist.SpO2, FCO72200435, 453564621801, 453564241901, kujuga.SpO2, 453564483321, FC2020, 453564621791 and 1 more |
| Date | Jan 1, 2019 |
| Regulator page | terviseamet.ee |
At a glance
- No Recall
- No Field safety notice
- 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