International safety notice
Edwards Lifesciences Miller, Fogarty atrioseptostoomiakateetrid - raskused ballooni tühjendamisel, ballooni purunemine või lahtitulemine
Estonia / EMDDB · EST · Apr 1, 2019
Key facts
| Title | Edwards Lifesciences Miller, Fogarty atrioseptostoomiakateetrid - raskused ballooni tühjendamisel, ballooni purunemine või lahtitulemine |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Edwards Lifesciences Miller, Fogarty atrioseptostoomiakateetrid |
| Manufacturer | EDWARDS LIFESCIENCES MILLER FOGARTY ATRIOSEPTOSTOOMIAKATEETRID |
| Models | 830515F, 830705F |
| Date | Apr 1, 2019 |
| Regulator page | terviseamet.ee |
At a glance
- No Recall
- No 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