International safety notice
Sistema de imagen intraoperatoria O-arm® 1000: Ref. BI70000027, Ref. BI70000027R, Ref. BI70000027100, Ref. BI70000027100R, Ref. BI70000027120, Ref. BI70000027120R, Ref. BI70000027230, Ref. BI70000027230R, Ref. BI70000027GER, Ref. BI70000027GERR
Spain / AEMPS · ESP · Oct 4, 2018
Key facts
| Title | Sistema de imagen intraoperatoria O-arm® 1000: Ref. BI70000027, Ref. BI70000027R, Ref. BI70000027100, Ref. BI70000027100R, Ref. BI70000027120, Ref. BI70000027120R, Ref. BI70000027230, Ref. BI70000027230R, Ref. BI70000027GER, Ref. BI70000027GERR |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistema de imagen intraoperatoria O-arm® 1000: Ref. BI70000027, Ref. BI70000027R, Ref. BI70000027100, Ref. BI70000027100R, Ref. BI70000027120, Ref. BI70000027120R, Ref. BI70000027230, Ref. BI70000027230R, Ref. BI70000027GER, Ref. BI70000027GERR |
| Manufacturer | Medtronic Navigation, Inc., Estados Unidos |
| Models | P9ZCKGCD19, BI70000027, BI70000027120R, 28022, 91.822.52.89, BI70000027GERR, BI70000027230R, 3.1.7, 48011, BI70000027230R, BI70000027120, BI70000027GER and 9 more |
| Event type | Safety Notice |
| Date | Oct 4, 2018 |
At a glance
- No Recall
- Yes 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