International safety notice
Axor II, componente del sistema OPRA. Referencia 1288
Spain / AEMPS · ESP · Nov 17, 2021
Key facts
| Title | Axor II, componente del sistema OPRA. Referencia 1288 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Axor II, componente del sistema OPRA. Referencia 1288 |
| Manufacturer | Integrum AB, Suecia |
| Models | 2021-10-06, 73307, 2021-634, 556407-3145, 011496, SE-431, 28022, 787684, 91.822.52.89 |
| Event type | Safety Notice |
| Date | Nov 17, 2021 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models 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