International safety notice
Urgent Field Safety Notice for COBRA Fusion 150 Minimally Invasive Ablation System by AtriCure, Inc.
Germany / BfArM · DEU · Feb 19, 2019
Key facts
| Title | Urgent Field Safety Notice for COBRA Fusion 150 Minimally Invasive Ablation System by AtriCure, Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | COBRA Fusion 150 Minimally Invasive Ablation System |
| Manufacturer | AtriCure, Inc. |
| Models | 2ETHYLHEXYL, EN60601-1-1, 513-895-9085, 700-001, CHADS2, 700-001MI, 1-METER, 12-FOOT, 700-004, 700-002, 1-513-755-4100, 513-755-4100 and 15 more |
| Date | Feb 19, 2019 |
| Regulator page | bfarm.de |
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