International safety notice
Dispositivos de anestesia Aespire 7100/Carestation (versión de software 1.x), Dispositivos de anestesia Aestiva 7100 (versión de software 1.x), Dispositivos de anestesia Aestiva 7900 (versión de software 1.x, 2.x y 3.x),Dispositivos anestesia Aestiva MRI
Spain / AEMPS · ESP · Sep 24, 2019
Key facts
| Title | Dispositivos de anestesia Aespire 7100/Carestation (versión de software 1.x), Dispositivos de anestesia Aestiva 7100 (versión de software 1.x), Dispositivos de anestesia Aestiva 7900 (versión de software 1.x, 2.x y 3.x),Dispositivos anestesia Aestiva MRI |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Dispositivos de anestesia Aespire 7100/Carestation (versión de software 1.x), Dispositivos de anestesia Aestiva 7100 (versión de software 1.x), Dispositivos de anestesia Aestiva 7900 (versión de software 1.x, 2.x y 3.x),Dispositivos anestesia Aestiva MRI |
| Manufacturer | Datex-Ohmeda, Inc., EEUU. |
| Models | 91.822.52.89, 2019-522, 35-37, 54541, 34101, 2014.DISPOSITIVOS, RECALL34101.CYBERSECURITY, 28022, 28023, 53188, ICSMA-19-190-01, 2004.DISPOSITIVOS and 1 more |
| Event type | Safety Notice |
| Date | Sep 24, 2019 |
At a glance
- No Recall
- Yes 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