International safety notice
Common name: Anesthesia system Sales name: (1)9100c NXT series (2) Avance CS2 (3) Avance Care Station (4) Acis (5) Estiva 7900 (6) Estiva Compact (7) Estiva/5 MRI (8) Estiva 7100 (9) Espire (10)Espire 7900 (11) Espire View
Japan / PMDA Recalls · JPN · Sep 6, 2021
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | Common name: Anesthesia system Sales name: (1)9100c NXT series (2) Avance CS2 (3) Avance Care Station (4) Acis (5) Estiva 7900 (6) Estiva Compact (7) Estiva/5 MRI (8) Estiva 7100 (9) Espire (10)Espire 7900 (11) Espire View |
| Manufacturer | GE Healthcare Japan Co., Ltd. |
| Models | AMXR01109, APHR00309, APKZ00402, AMRM01229, AMRQ00265, ANCS00162, APHU00262, AMRF00129, AMRN00681, AMVJ00648, AMX10500859WA, AMRN01265 and 6557 more |
| Date | Sep 6, 2021 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 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