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enVVeno Medical Presents Positive Preliminary Device Related Material Adverse Event (MAE) Data from the VenoValve Pivotal Trial at the 50th Annual VEITH Symposium

enVVeno Medical Presents Positive Preliminary Device Related Material Adverse Event (MAE) Data from the VenoValve Pivotal Trial at the 50th Annual VEITH Symposium
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New York , United States , Jenene Thomas , Robert Berman , Vveno Medical Corporation The Company , Drug Administration , Vveno Medical Corporation , Clinical Events Committee , Exchange Commission , Vveno Medical Corporation Nasdaq , Pulmonary Embolisms Occurring During , Fully Enrolled , Medical Corporation , Material Adverse Event , Chronic Venous Insufficiency , Data Safety Monitoring Board , Private Securities Litigation Reform Act ,

enVVeno Medical Presents Positive Preliminary Device Related Material Adverse Event (MAE) Data from the VenoValve Pivotal Trial at the 50th Annual VEITH Symposium

enVVeno Medical Presents Positive Preliminary Device Related Material Adverse Event (MAE) Data from the VenoValve Pivotal Trial at the 50th Annual VEITH Symposium
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United States , New York , Robert Berman , Jenene Thomas , Vveno Medical Corporation The Company , Vveno Medical Corporation , Drug Administration , Exchange Commission , Clinical Events Committee , Vveno Medical Corporation Nasdaq , Pulmonary Embolisms Occurring During , Fully Enrolled , Medical Corporation , Material Adverse Event , Chronic Venous Insufficiency , Data Safety Monitoring Board , Private Securities Litigation Reform Act ,

enVVeno Medical Presents Positive Preliminary Device Related Material Adverse Event (MAE) Data from the VenoValve Pivotal Trial at the 50th Annual VEITH Symposium

enVVeno Medical Presents Positive Preliminary Device Related Material Adverse Event (MAE) Data from the VenoValve Pivotal Trial at the 50th Annual VEITH Symposium
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United States , New York , Robert Berman , Jenene Thomas , Clinical Events Committee , Drug Administration , Vveno Medical Corporation Nasdaq , Vveno Medical Corporation The Company , Vveno Medical Corporation , Exchange Commission , Pulmonary Embolisms Occurring During , Fully Enrolled , Medical Corporation , Material Adverse Event , Chronic Venous Insufficiency , Data Safety Monitoring Board , Private Securities Litigation Reform Act ,

InspireMD Presents Positive 30-Day Follow-Up Results from the C-GUARDIANS U.S. Investigational Device Exemption (IDE) Clinical Trial at VIVA23

InspireMD Presents Positive 30-Day Follow-Up Results from the C-GUARDIANS U.S. Investigational Device Exemption (IDE) Clinical Trial at VIVA23
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United States , Marvin Slosman , Chuck Padala , Chris Metzger , Las Vegas , Inspiremd Inc , Clinical Events Committee , Exchange Commission , Company Annual Report On Form , Day Follow Up Results , Device Exemption , Clinical Trial , Embolic Prevention Stent System , Vascular Interventional Advances , System Vascular Chief , Carotid Stent System , Premarket Approval , Annual Report , Quarterly Reports ,

InspireMD Presents Positive 30-Day Follow-Up Results from the C-GUARDIANS U.S. Investigational Device Exemption (IDE) Clinical Trial at VIVA23

TEL AVIV, Israel and MIAMI, Nov. 01, 2023 InspireMD, Inc. , developer of the CGuard™ Embolic Prevention Stent System for the prevention of stroke, today presented 30-day results from the. ....

United States , Las Vegas , Chris Metzger , Marvin Slosman , Chuck Padala , Globenewswire Inc , Inspiremd Inc , Exchange Commission , Company Annual Report On Form , Clinical Events Committee , Embolic Prevention Stent System , Device Exemption , Vascular Interventional Advances , System Vascular Chief , Carotid Stent System , Premarket Approval , Annual Report , Quarterly Reports ,