International safety notice
Abbott Alinity m SARS-CoV-2 AMP Kit, m Resp-4-Plex AMP Kit - UUENDATUD parandused ülekande ja valepositiivsete tulemuste vähendamiseks
Estonia / EMDDB · EST · Apr 1, 2022
Key facts
| Title | Abbott Alinity m SARS-CoV-2 AMP Kit, m Resp-4-Plex AMP Kit - UUENDATUD parandused ülekande ja valepositiivsete tulemuste vähendamiseks |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Abbott Alinity m SARS-CoV-2 AMP Kit, m Resp-4-Plex AMP Kit |
| Manufacturer | ABBOTT ALINITY M SARSCOV2 AMP KIT M RESP4PLEX AMP KIT |
| Models | 09N78-090, Resp-4-P1ex, 09N79-090, 0.0016, 60018, 00884999049963, 09N79-01D, FA-AM-SEP2021-260Bv2, 09N78-01E, 09N78-091, 0.0078, FA-AM-SEP2021-260 and 5 more |
| Date | Apr 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