International safety notice
Philips steriliseeritavad kehasisesed defibrillaatorilabad - töökindluse perioodilise kontrolli vajadus
Estonia / EMDDB · EST · May 1, 2020
Key facts
| Title | Philips steriliseeritavad kehasisesed defibrillaatorilabad - töökindluse perioodilise kontrolli vajadus |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Philips steriliseeritavad kehasisesed defibrillaatorilabad |
| Manufacturer | PHILIPS STERILISEERITAVAD KEHASISESED DEFIBRILLAATORILABAD |
| Models | M4743A, M4744A, FSN86100197A, M4742A, M1742A, 76401, M1743A, M1741A, M1744A, M1744ALülitatav, M4744AMõjutatud, M4741A |
| Date | May 1, 2020 |
| Regulator page | terviseamet.ee |
At a glance
- No Recall
- No Field safety notice
- 10–99 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