International safety notice
Sistemas Allura Xper
Spain / AEMPS · ESP · Mar 29, 2019
Key facts
| Title | Sistemas Allura Xper |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistemas Allura Xper |
| Manufacturer | Philips Medical Systems Nederland BV, Holanda. |
| Models | 20722058, 722026, 722010, 5.416, 722003, A-28017143, 51269, 722001, 722012, 28022, 28050, 91.822.52.89 and 8 more |
| Event type | Safety Notice |
| Date | Mar 29, 2019 |
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