International safety notice
Getinge Atrium Advanta V12 Covered Stent System - ballooni või kateetri osade eraldumine
Estonia / EMDDB · EST · Mar 1, 2022
Key facts
| Title | Getinge Atrium Advanta V12 Covered Stent System - ballooni või kateetri osade eraldumine |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Getinge Atrium Advanta V12 Covered Stent System |
| Manufacturer | GETINGE ATRIUM ADVANTA V12 COVERED STENT SYSTEM |
| Models | 85396, 85338, 85325, 85331, 85336, 85335, 85343, 85364, 85353, 85392, 85370, 85352 and 42 more |
| Date | Mar 1, 2022 |
| Regulator page | terviseamet.ee |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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