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enVastTM

REDEFINING CORONARY THROMBECTOMY

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

ENVAST DESIGNED FOR RAPID, HI-FLOW REPERFUSION

ENVAST
IN ACTION

FOR MORE CASES

Comprehensive Clot Removal

  • full range of clots
  • larger volumes of clot

Proximal-to-Distal
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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Indications, Safety, and Warnings