International safety notice
Catéter guía MIVI Super 90, referencias MIA-9080S-E, MIA-9090S-E, MIA-9095S-E
Spain / AEMPS · ESP · Aug 23, 2021
Key facts
| Title | Catéter guía MIVI Super 90, referencias MIA-9080S-E, MIA-9090S-E, MIA-9095S-E |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Catéter guía MIVI Super 90, referencias MIA-9080S-E, MIA-9090S-E, MIA-9095S-E |
| Manufacturer | MIVI Neuroscience, Inc., EEUU. |
| Models | M20110005, 01-952-944-3834, M21010008, M21060017, MIA-9090S-E, M21060016, M21030015, M21050014, M21030014, M21050015, M21060003, M20090012 and 28 more |
| Event type | Safety Notice |
| Date | Aug 23, 2021 |
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