Discover

enVastTM

ENGINEERED FOR
CORONARY THROMBECTOMY

enVast is the first and only CE-approved and FDA-cleared large thrombus burden retriever in patients with coronary occlusions.

LINK TO IFU
LINK TO IFU

ENVAST EFFECTIVE & SAFE

Equipped with Drop Zone technology, the enVast coronary thrombectomy system has been proven to remove large thrombus burden (LTB) and create immediate reperfusion in 85% of cases. (n = 61)

EFFECTIVE

(core-lab adjudicated)

72%

MBG 2-3 after enVast

85%

immediate reperfusion at enVast deployment

90%

TIMI 3
after enVast

98%

TIMI 3
end of PCI

SAFE

Procedural Outcomes

0

  • coronary dissection
  • coronary perforation
  • cardiac tamponade
  • life-threatening arrhythmia
  • flow-limiting spasm

1.6%

coronary embolization (all resolved)

Clinical Outcomes – 30 Days

0

  • stroke
  • recurrent MI
  • bleeding BAARC 3 or 5

3.3%

cardiovascular death (patients were in cardiogenic shock at admission)

LINK TO PUBLICATION

ENVAST DESIGNED FOR
WALL APPOSITION AND FULL CIRCUMFERENTIAL CLOT ENGAGEMENT

ENVAST IN ACTION

FOR MORE CASES

Comprehensive Clot Removal

  • full range of clots
  • larger volumes of clot

End-to-End
Clot Engagement

designed to mitigate distal embolization and stroke risk

Engineered for
Vessel-wall Conformity

  • adapts to anatomical challenges
  • allows complete clot integration

INVESTING IN CLINICAL SCIENCE

Vesalio is sponsoring the NATURE study, a randomized, multi-center clinical trial, comparing the safety and efficacy of enVast™ as an adjunct to conventional intervention versus the standard of care in MI patients with large thrombus burden.

clinicaltrials.gov ID NCT04969471

FOR MORE INFORMATION

“enVast could provide a new therapeutic opportunity for myocardial infarct patients with large thrombus burden, who still represent a major challenge for procedural success and long-term outcomes.”

Prof Dr Marco Valgimigli

Istituto Cardiocentro Ticino, Lugano, Switzerland

CHOOSE
TO REMOVE

Precaution: The safety and effectiveness of this device for use in the treatment of ST-Elevation Myocardial Infarction (STEMI) have not been established. Complications from the use of this device in this manner could lead to death, permanent impairment, and/or the need for emergency medical intervention

Do The
Drop Zone

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