International safety notice
Abbott Alinity m System - UUENDATUD viivitatud või valed testitulemused
Estonia / EMDDB · EST · Feb 1, 2022
Key facts
| Title | Abbott Alinity m System - UUENDATUD viivitatud või valed testitulemused |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Abbott Alinity m System |
| Manufacturer | ABBOTT ALINITY M SYSTEM |
| Models | 00834999043034, 640-060, 60018, 03NE3-002, FÄ-AM-DEC2021-264Bv2, 08N53-ct2, 543-3, FA-AM-DEC2021-262, Resp-4-Plex, 2=tenuia, nbD0-t, 38-N53-c22 and 9 more |
| Date | Feb 1, 2022 |
| 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