International safety notice
GE Healthcare EKG kaablid ja juhtmed – võimalik energia vähenemine defibrillatsiooni ajal
Estonia / EMDDB · EST · Jun 1, 2019
Key facts
| Title | GE Healthcare EKG kaablid ja juhtmed – võimalik energia vähenemine defibrillatsiooni ajal |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | GE Healthcare EKG kaablid ja juhtmed – võimalik energia vähenemine defibrillatsiooni ajal |
| Manufacturer | GE HEALTHCARE EKG KAABLID JA JUHTMED VÕIMALIK ENERGIA VÄHENEMINE DEFIBRILLATSIOONI AJAL |
| Models | 2106389-006, 2106396-001, 2106310-002, 00840682140379, 2106389-001, 00840682139892, 2106392-004, 00840682140461, 2106383-003, 2106388-101, 00840682139823, 00840682139687 and 173 more |
| Date | Jun 1, 2019 |
| 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