International safety notice
Ensayo de estradiol (estradiol-17b, E2) en suero, código E2, que utiliza los analizadores IMMULITE, IMMULITE 1000, IMMULITE 2000 e IMMULITE 2000 XPi,
Spain / AEMPS · ESP · Jul 1, 2021
Key facts
| Title | Ensayo de estradiol (estradiol-17b, E2) en suero, código E2, que utiliza los analizadores IMMULITE, IMMULITE 1000, IMMULITE 2000 e IMMULITE 2000 XPi, |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Ensayo de estradiol (estradiol-17b, E2) en suero, código E2, que utiliza los analizadores IMMULITE, IMMULITE 1000, IMMULITE 2000 e IMMULITE 2000 XPi, |
| Manufacturer | Siemens Healthcare Diagnostics Products Limited, Reino Unido. |
| Models | IMC20-01.C.OUS, 2021-378, 501-553, 28022, 501-557, 91.822.52.89, 2021-087, 2020-106, 28906, 58082, 10381132, 2021PUEDE and 4 more |
| Event type | Safety Notice |
| Date | Jul 1, 2021 |
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