Graft, Vascular, Synthetic/biologic Composite
Vascutek Ltd.'s record for this product code
MDR events24All time
Recalls2All time
510(k) clearances0All time
Recent MDR events
24 adverse event reports on file
- GESLOFTJul 26, 2022Injury9612515-2022-00009
- GELSOFTNov 16, 2021Malfunction9612515-2021-00024
- GELSOFTApr 28, 2021Malfunction9612515-2021-00013
- GELSOFTMar 16, 2021Malfunction9612515-2021-00010
- GELSOFTJun 26, 2019Malfunction9612515-2019-00012
- GELSOFTJun 26, 2019Malfunction9612515-2019-00010
- GELSOFTJun 26, 2019Malfunction9612515-2019-00009
- GELSOFTJun 26, 2019Malfunction9612515-2019-00013
- GELSOFTMar 14, 2019Malfunction9612515-2019-00003
- GELSOFTOct 17, 2018Malfunction9612515-2018-00020
Recalls
2 recall events for this product code
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for Vascutek Ltd. under this product code.