International safety notice
Sistema de imagen intraoperatoria O-Arm 1000
Spain / AEMPS · ESP · Jun 14, 2019
Key facts
| Title | Sistema de imagen intraoperatoria O-Arm 1000 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistema de imagen intraoperatoria O-Arm 1000 |
| Manufacturer | Medtronic Navigation, Inc., EEUU |
| Models | UP-980, 60601-1-1, FIGURA4-6, TABLA3-2.FUNCIONES, FIGURA3-12, 1-866-843-6276, TABLA9-3.VERIFICACIONES, FIGURA5-21, FIGURA7-5, 720-890-3160, FIGURA5-11, 1020.32 and 268 more |
| Event type | Safety Notice |
| Date | Jun 14, 2019 |
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