International safety notice
Philips Medical Systems Nederland BV Philips Azurion, Philips Allura -l-kaare pöördkate võib kukkude süsteemidele
Estonia / EMDDB · EST · Nov 1, 2023
Key facts
| Title | Philips Medical Systems Nederland BV Philips Azurion, Philips Allura -l-kaare pöördkate võib kukkude süsteemidele |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Philips Medical Systems Nederland BV Philips Azurion, Philips Allura -l-kaare pöördkate võib kukkude süsteemidele |
| Manufacturer | PHILIPS MEDICAL SYSTEMS NEDERLAND BV PHILIPS AZURION PHILIPS ALLURA LKAARE PÖÖRDKATE VÕIB KUKKUDE SÜSTEEMIDELE |
| Models | 722224, 722028, 722015, 51naela, 722001, 722016, H5000, 722033, 722078, 722035, 2022-IGT-BST-002, 722003 and 19 more |
| Date | Nov 1, 2023 |
| Regulator page | terviseamet.ee |
At a glance
- No Recall
- No 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