International safety notice
Seegene Inc. Allplex™ Respiratory Panel 1 - tundlikkuse vähenemine sptesiifilise tüve tõttu
Estonia / EMDDB · EST · May 1, 2024
Key facts
| Title | Seegene Inc. Allplex™ Respiratory Panel 1 - tundlikkuse vähenemine sptesiifilise tüve tõttu |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Seegene Inc. Allplex™ Respiratory Panel 1 |
| Manufacturer | SEEGENE INC ALLPLEX RESPIRATORY PANEL |
| Models | 6B.1A.5a.2a.l, 6B.1A.5a.2a.1, RP9801Xja, A-Hlpdm09, RV10349Z, 6B.1A.5a.2a, SARS-CoV-2, RP9801Y, Hipdm09, 58.61, 79.14, 82-2-2240-4000 and 7 more |
| Date | May 1, 2024 |
| 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