International safety notice
O-arm® 1000 Imaging System
Ireland / HPRA · IRL · Jun 6, 2019
Key facts
| Title | O-arm® 1000 Imaging System |
|---|---|
| Regulator | Ireland / HPRA |
| Country | IRL |
| Brand | O-arm® 1000 Imaging System |
| Manufacturer | Medtronic Navigation, Inc. |
| Models | BI70000027230, BI-700-00028-120R, BI70000027GER, BI-700-00027-100R, BI70000027100R, BI-700-00028-120, BI70000027120R, BI-700-00027-230, BI70000028100, BI-700-00027GERR, BI70000028230R, BI-700-00027-230R and 23 more |
| Event type | Safety Notice |
| Date | Jun 6, 2019 |
| Regulator page | hpra.ie |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models 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