Intended for healthcare professionals

ENTERPRISE™2 Vascular Reconstruction Device

Stability, Conformability and Ease of Use.

Features & benefits

ENTERPRISE™2 Vascular Reconstruction Device

Stability

Higher Radial Resistive Force than Neuroform®, LVIS™Jr. and Solitaire™ 2/FR stents*


Higher Chronic Outward Force than LVIS™Jr. and Solitaire™2/FR stents**


Higher Point Load Force than Neuroform®, LVIS™Jr. and Solitaire™ stents***

ENTERPRISE™2 Vascular Reconstruction Device

Conformability

Better wall apposition in curved vessels than ENTERPRISE® stenti


Excellent kink resistance in comparison to ENTERPRISE® stentii

ENTERPRISE™2 Vascular Reconstruction Device

Ease of use

Can recapture and redeploy after partial deployment with less foreshortening than LVIS™Jr. and Solitaire™2/FR stentsiii


Radiopaque markers for visibility during and after device deployment


Introducer with tapered distal end and flush ports


Compatibility with Prowler Select™ Plus 0.021 inch ID microcatheters

Related products

Prowler® EX Microcatheter

Prowler® EX Microcatheter

The PROWLER® EX Microcatheter is a variable stiffness, single lumen catheter designed to access small, tortuous vasculature. The catheter has a hydrophilic coating to provide lubricity for navigation of vessels. The inner lumen is lined with lubricious PTFE to facilitate movement of guidewires and other devices.

TRUFILL™ n-BCA Liquid Embolic System

TRUFILL™ n-BCA Liquid Embolic System

Now available as PROCEDURAL SET

References

Important safety information / Essential product information​

Important information: Prior to use, refer to the instructions for use supplied with this device for indications, contraindications, side effects, warnings and precautions.
Caution: US law restricts this device to sale by or on the order of a physician.
This site is published by CERENOVUS which is solely responsible for its contents. It is intended for visitors from the United States.

Third party trademarks used herein are the properties of their respective owners.
* Based on 2015 benchtop testing of average radial resistive force at 3mm diameter.
** Based on benchtop testing of average Chronic Outward Force of each stent at 3mm diameter.
*** Based on bench top testing Windchill Document #103111155 analyzing the mean point load force on the body of the stent.
i. Based on the findings from the in vivo study Li Z, Xuan J, Fang X, Zhao X, ZhangB et al. Comparison of Enterprise stent 2 with 1 in assisting coiling of ruptured aneurysms: A real-world study. J Comp Eff Res 11(12): 2022. Pg884. Paragraph 3.
ii. Based on an in vitro study comparing Enterprise VRD to Enterprise VRD 2: Li Z, Xuan J, Fang X, Zhao X, ZhangB et al. (2022) Comparison of Enterprise stent 2 with 1 in assisting coiling of ruptured aneurysms: A real-world study. J Comp Eff Res 11(12).
iii. Based on Competitive Performance Testing Windchill Document #103111155.
iv. Based from bench top study Jacobs Institute. ENTERPRISE® 2 and Atlas Flow Characterization Study. Revision A. RPT-24-007. June 11, 2024 1. Li Z, Xuan J, Fang X, Zhao X, ZhangB et al. Comparison of Enterprise stent 2 with 1 in assisting coiling of ruptured aneurysms: A real-world study. J Comp Eff Res 11(12): 2022. Pg884.

HUMANITARIAN DEVICE (USA ONLY): The CERENOVUS ENTERPRISE™ Vascular Reconstruction Device and Delivery System is authorized by Federal Law for use
with embolic coils for the treatment of wide-neck, intracranial, saccular or fusiform aneurysms arising from a parent vessel with a diameter of ≥ 2.5 mm and ≤ 4
mm. Wide-neck is defined as having a neck width ≥4 mm or a dome-to-neck ratio < 2. The effectiveness of this device for this use has not been demonstrated.

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