International safety notice
Atellica IM Enhanced Estradiol (eE2) 100T, SMN 10995561, Atellica IM Enhanced Estradiol (eE2) 500T, SMN 10995562, ADVIA Centaur Enhanced Estradiol (eE2) 100T, SMN 10490889 y ADVIA Centaur Enhanced Estradiol (eE2) 500T, SMN 10491445
Spain / AEMPS · ESP · Mar 15, 2022
Key facts
| Title | Atellica IM Enhanced Estradiol (eE2) 100T, SMN 10995561, Atellica IM Enhanced Estradiol (eE2) 500T, SMN 10995562, ADVIA Centaur Enhanced Estradiol (eE2) 100T, SMN 10490889 y ADVIA Centaur Enhanced Estradiol (eE2) 500T, SMN 10491445 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Atellica IM Enhanced Estradiol (eE2) 100T, SMN 10995561, Atellica IM Enhanced Estradiol (eE2) 500T, SMN 10995562, ADVIA Centaur Enhanced Estradiol (eE2) 100T, SMN 10490889 y ADVIA Centaur Enhanced Estradiol (eE2) 500T, SMN 10491445 |
| Manufacturer | Siemens Healthcare Diagnostics Inc., EEUU. |
| Models | 10995562, 10491445, 78069, 28022, 2022-133, 22-03.A.OUS, 91.822.52.89, 28906, 10995561, 10490889ADVIA, 10995561ATELLICA, 10995562ADVIA and 1 more |
| Event type | Safety Notice |
| Date | Mar 15, 2022 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 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