International safety notice
Medtronic CoreValve Evolut R, PRO Transcatheter Aortic Valve - kasutusjuhendi täiendamine
Estonia / EMDDB · EST · Oct 1, 2020
Key facts
| Title | Medtronic CoreValve Evolut R, PRO Transcatheter Aortic Valve - kasutusjuhendi täiendamine |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Medtronic CoreValve Evolut R, PRO Transcatheter Aortic Valve |
| Manufacturer | MEDTRONIC COREVALVE EVOLUT R PRO TRANSCATHETER AORTIC VALVE |
| Models | EVOLUTPRO-23, EVOLUTR-23, 0.020, EVOLUTPRO-26, FA935, EVOLUTPRO-29, EVOLUTR-26, EVOLUTR-34, EVOLUTR-29 |
| Date | Oct 1, 2020 |
| Regulator page | terviseamet.ee |
At a glance
- No Recall
- No 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