International safety notice
Analizador Erytra-Eflexis, código del producto 210600 y UDI 08436583730942
Spain / AEMPS · ESP · Aug 23, 2024
Key facts
| Title | Analizador Erytra-Eflexis, código del producto 210600 y UDI 08436583730942 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Analizador Erytra-Eflexis, código del producto 210600 y UDI 08436583730942 |
| Manufacturer | Diagnostic Grifols S.A., España. |
| Models | 3.1.0, 08436583730942, 109806, 210600, 28022, 1.2.0, 91.822.52.89, 08150, 2024-467, 3.2.0 |
| Event type | Safety Notice |
| Date | Aug 23, 2024 |
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