International safety notice
Productos de embolización endovascular AZUR: Sistemas de espiral periférica AZUR desacoplable 18, Sistemas de espiral periférica AZUR desacoplable 35
Spain / AEMPS · ESP · Dec 11, 2019
Key facts
| Title | Productos de embolización endovascular AZUR: Sistemas de espiral periférica AZUR desacoplable 18, Sistemas de espiral periférica AZUR desacoplable 35 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Productos de embolización endovascular AZUR: Sistemas de espiral periférica AZUR desacoplable 18, Sistemas de espiral periférica AZUR desacoplable 35 |
| Manufacturer | MicroVention Inc, EEUU |
| Models | 00816777024367, 1903135ZA, 00816777024374, 190506582, 1905135J2, 1904265Z8, 45-751324, 19030456J, 1904175J5, 00810170018053, 45-450405, 00810170014932 and 332 more |
| Event type | Safety Notice |
| Date | Dec 11, 2019 |
At a glance
- No Recall
- Yes 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