International safety notice
Philips Medical Systems Nederland BV Allura Xper, Azurion, Integris, Multidiagnost Eleva - kaablivooliku kanduri võimalik eraldumine
Estonia / EMDDB · EST · Sep 1, 2024
Key facts
| Title | Philips Medical Systems Nederland BV Allura Xper, Azurion, Integris, Multidiagnost Eleva - kaablivooliku kanduri võimalik eraldumine |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Philips Medical Systems Nederland BV Allura Xper, Azurion, Integris, Multidiagnost Eleva |
| Manufacturer | PHILIPS MEDICAL SYSTEMS NEDERLAND BV ALLURA XPER AZURION INTEGRIS MULTIDIAGNOST ELEVA |
| Models | 722028, k6iki, n6uetekohaselt, 722017, t6rgeteta, 722235, 722012, 722039, p5rutused, 722281, 722234, 722006 and 92 more |
| Date | Sep 1, 2024 |
| Regulator page | terviseamet.ee |
At a glance
- No Recall
- No Field safety notice
- 10–99 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