International safety notice
Carescape One utilizado con el portamódulo F2-01 (con referencia 5861293).
Spain / AEMPS · ESP · Feb 3, 2023
Key facts
| Title | Carescape One utilizado con el portamódulo F2-01 (con referencia 5861293). |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Carescape One utilizado con el portamódulo F2-01 (con referencia 5861293). |
| Manufacturer | GE Healthcare Finland Oy, Finlandia |
| Models | 5861293, 36154, F2-01, 118226, 28022, 91.822.52.89, 2023-045, RECALL.36154, 28023, 00195278524089, 89758 |
| Event type | Safety Notice |
| Date | Feb 3, 2023 |
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