International safety notice
Elektromechanické zdravotnické prostředky
Czech / Ksrzis · CZE · Feb 13, 2019
Key facts
| Title | Elektromechanické zdravotnické prostředky |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | Philips Hemodynamic Application R1.0 (Hemodynamická aplikace Philips R1.0.1) |
| Manufacturer | Philips Medical Systems Nederland B. V., Nizozemsko |
| Models | 722463, 1.0.1, 2018-1GTBST-019, R1.0.1, 002010 |
| Event type | Safety Notice |
| Date | Feb 13, 2019 |
| Regulator page | eregpublicsecure.ksrzis.cz |
At a glance
- No Recall
- Yes 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