International safety notice
Field Safety Notice for Astral 100 and Astral 150 as well as Astral 100 and Astral 150 devices with SR1.1 software (SX544-0301), ResMed Ltd. / ResMed Paris
Germany / BfArM · DEU · Feb 3, 2016
Key facts
| Title | Field Safety Notice for Astral 100 and Astral 150 as well as Astral 100 and Astral 150 devices with SR1.1 software (SX544-0301), ResMed Ltd. / ResMed Paris |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Astral 100 and Astral 150 as well as Astral 100 and Astral 150 devices with SR1.1 software (SX544-0301), ResMed Ltd. / ResMed Paris |
| Manufacturer | Field Safety Notice for Astral 100 and Astral 150 as well as Astral 100 and Astral 150 devices with SR1.1 software (SX544-0301), ResMed Ltd. / ResMed Paris |
| Models | FSN1512002, F-77550, SX544-0301, FSN1504001, SX5440401, SR1.1 |
| Date | Feb 3, 2016 |
| Regulator page | bfarm.de |
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