International safety notice
Philips Respironics All BiPap A30, A30 EFL, A30 Hybrid, A40, A40 EFL and A40 Pro Devices - mittetöötav alarm
Estonia / EMDDB · EST · Jun 1, 2024
Key facts
| Title | Philips Respironics All BiPap A30, A30 EFL, A30 Hybrid, A40, A40 EFL and A40 Pro Devices - mittetöötav alarm |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Philips Respironics All BiPap A30, A30 EFL, A30 Hybrid, A40, A40 EFL and A40 Pro Devices |
| Manufacturer | PHILIPS RESPIRONICS ALL BIPAP A30 A30 EFL A30 HYBRID A40 A40 EFL AND A40 PRO DEVICES |
| Models | 0.00088, 2023-CC-SRC-039, 2023-CC, 15668, 24-hour, 2023-CC-SRC-039-B, SRC-039-B |
| Date | Jun 1, 2024 |
| Regulator page | terviseamet.ee |
At a glance
- No Recall
- No 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