International safety notice
Sistemas Philips Allura Exper, Integris, MultiDiagnost Eleva y OmniDiagnost Eleva, entregados a partir de 2010 hasta el 2014 inclusive
Spain / AEMPS · ESP · Jan 22, 2020
Key facts
| Title | Sistemas Philips Allura Exper, Integris, MultiDiagnost Eleva y OmniDiagnost Eleva, entregados a partir de 2010 hasta el 2014 inclusive |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistemas Philips Allura Exper, Integris, MultiDiagnost Eleva y OmniDiagnost Eleva, entregados a partir de 2010 hasta el 2014 inclusive |
| Manufacturer | Philips Medical Systems Nederland BV, Holanda |
| Models | 2020-032, FCO70800160, 2018-IGTBST-015, 5.416, 91.822.52.89, 28050, FCO70800159, FCO72200436, 57142, 28022, A-28017143 |
| Event type | Safety Notice |
| Date | Jan 22, 2020 |
At a glance
- No Recall
- Yes Field safety notice
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