International safety notice
Urgent Field Safety Notice for NEXUS Aortic Arch Stent Graft System by Endospan Ltd.
Germany / BfArM · DEU · Jul 21, 2022
Key facts
| Title | Urgent Field Safety Notice for NEXUS Aortic Arch Stent Graft System by Endospan Ltd. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | NEXUS Aortic Arch Stent Graft System |
| Manufacturer | Endospan Ltd. |
| Models | IP-21-0006, IN-21-0007, MK-21-0002, KW-21-0006, IV-21-0007, MR-21-0001, OE-19-0004, ML-21-0017, IV-21-0004, KY-20-0005, MQ-20-0001, KW-21-0005 and 85 more |
| Date | Jul 21, 2022 |
| Regulator page | bfarm.de |
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