International safety notice
Abbott Alinity m SARS-CoV-2 AMP Kit, m Resp-4-Plex AMP Kit - võimalikud valepositivsed tulemused
Estonia / EMDDB · EST · Sep 1, 2021
Key facts
| Title | Abbott Alinity m SARS-CoV-2 AMP Kit, m Resp-4-Plex AMP Kit - võimalikud valepositivsed tulemused |
|---|---|
| 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 | 514074, 512898, 520596, 517139, 515652, 220518, 519091, 211106, 515053, 511505, 520388, 210918 and 136 more |
| Date | Sep 1, 2021 |
| Regulator page | terviseamet.ee |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 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