Instruments, Surgical, Cardiovascular
Atrium Medical Corporation's record for this product code
MDR events6All time
Recalls0All time
510(k) clearances0All time
Recent MDR events
6 adverse event reports on file
- TUNNELER AV-1Sep 24, 2020Malfunction3011175548-2020-01164
- TUNNELERSep 3, 2020Injury3011175548-2020-01106
- GRAFTS ACCESSORIES TUNNELERSDec 9, 2019Malfunction3011175548-2019-01218
- GRAFTS ACCESSORIES TUNNELERSOct 7, 2019Malfunction3011175548-2019-01078
- ATRIUM VEIN GRAFTTUNNELING SYSTEMJul 27, 2016Death1219977-2016-00165
- TUNNELER RX1 6 AV-1Apr 17, 2013Malfunction1219977-2013-00027
Recalls
0 recall events for this product code
No recalls on file for Atrium Medical Corporation under this product code.
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for Atrium Medical Corporation under this product code.