International safety notice
ADVIA Centaur CA 19-9 (kit de 50 pruebas), SMN 10491379 y UDI 0063041457425723281516230630 y ADVIA Centaur CA 19-9 (kit de 250 pruebas), SMN 10491244 y UDI 0063041457402823280516230630
Spain / AEMPS · ESP · Oct 25, 2022
Key facts
| Title | ADVIA Centaur CA 19-9 (kit de 50 pruebas), SMN 10491379 y UDI 0063041457425723281516230630 y ADVIA Centaur CA 19-9 (kit de 250 pruebas), SMN 10491244 y UDI 0063041457402823280516230630 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | ADVIA Centaur CA 19-9 (kit de 50 pruebas), SMN 10491379 y UDI 0063041457425723281516230630 y ADVIA Centaur CA 19-9 (kit de 250 pruebas), SMN 10491244 y UDI 0063041457402823280516230630 |
| Manufacturer | Siemens Healthcare Diagnostics Inc, EEUU. |
| Models | 28022, 16-02.B.US, 28906, 30-06-2023, 88996, 0063041457402823280516230630, 36147, 16-02.A.OUS, 10491244, SMN10325894, 91.822.52.89, 0063041457425723281516230630ADVIA and 6 more |
| Event type | Safety Notice |
| Date | Oct 25, 2022 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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