International safety notice
Safety Notice for Aespire, Avance, Amingo and ADS180 Anaesthesia Machines, GE Healthcare
Germany / BfArM · DEU · Jun 2, 2010
Key facts
| Title | Safety Notice for Aespire, Avance, Amingo and ADS180 Anaesthesia Machines, GE Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Aespire, Avance, Amingo and ADS180 Anaesthesia Machines, GE Healthcare |
| Manufacturer | Safety Notice for Aespire, Avance, Amingo and ADS180 Anaesthesia Machines, GE Healthcare |
| Models | AMXL00100-AMXN01192, RP2130, 53226, ANBL00100-ANBN01719, 34029, AMXL01114, AMXM00476, ANCL00100-ANCN01565, AMXM01233, AMNM0100-AMNN00164, APHN00100-APHN00179, AMXN00302 and 1 more |
| Date | Jun 2, 2010 |
| Regulator page | bfarm.de |
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