Sirolimus-Eluting Bioresorbable Coronary Stent Implant

Product Details
Customization: Available
Type: Coronary Stents
Material: Fully Degradable Poly(L-Lactide)
Diamond Member Since 2024

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  • Overview
  • Product Description
  • FAQ
  • Ordering information
  • Product Parameters
Overview

Basic Info.

Model NO.
NeoVas
Ethylene Oxide Sterilization
Ethylene Oxide Sterilization
Quality Guarantee Period
One Year
Group
Adult
Logo Printing
Without Logo Printing
Origin
China
HS Code
9021900001

Product Description

Sirolimus-Eluting Bioresorbable Coronary Stent Implant
Product Description

 

       Stent Platform

  • Fully degradable poly(L-lactide)

  • Sine wave structure in space, In-phase peak-valley connection

       Drug coating

  • Fully degradable poly(D,L-lactide)

  • Effectively control sirolimus release rate
    Drug

  • Classical Sirolimus with dose of 15.3ug/mm

  • Inhibit the proliferation and migration of smooth muscle cells

  • Delivery system

  • Completely self-developed second-generation rapid-exchange balloon dilatation catheter

  • Superior pushability and crossability
     

    FAQ
     

    NeoVas RCT Study

    The study enrolled 560 subjects in 33 centers from China, Test group(NeoVas): 278 cases, Control group (Xience stent): 282 cases.

    Primary endpoint: the late lumen loss in one year follow-up
    Sirolimus-Eluting Bioresorbable Coronary Stent Implant
    The clinical result at one year follow-up
    Sirolimus-Eluting Bioresorbable Coronary Stent ImplantThe clinical result at Three year follow-up
    Sirolimus-Eluting Bioresorbable Coronary Stent Implant

    Conclusion:

    The clinical events rate for Neovas bioabsorbable stent is low, showed equal safety and effectiveness with Xience metal stent.

NeoVas OPC study

The study enrolled 1103 subjects in 45 centers from China, two year clinical follow-up study has been completed to date.

1-2 year follow-up result
Sirolimus-Eluting Bioresorbable Coronary Stent Implant

2 year stent thrombus: Compare with Absorb and Xience
Sirolimus-Eluting Bioresorbable Coronary Stent Implant

Conclusion:

2-year follow up Clinical results for 1103 subjects demonstrate that NeoVas bioresorbable stent has equal low clinical events rate. Compared with the first generation bioresorbable stent Absorb BVS, the clinical events rate has been obviously decreased, and it indicates that NeoVas performed favorable safety and effectiveness.

 

The Imaging study of the NeoVas Subgroup

The subgroup analyzed the imaging and function of 166 subjects from the randomized controlled study, 83 cases for test/control group.

Sirolimus-Eluting Bioresorbable Coronary Stent ImplantOCT: Study on stent absorption in 3 years
Sirolimus-Eluting Bioresorbable Coronary Stent Implant

Conclusion:

NeoVas subgroup of 3 years clinical imaging data shows vessel vasomotor function has been restored after 3 years implantation, superior to metal stent. Blood supply keeps at favorable level. Most stent was degraded and absorbed after 3 years.

 

The importance of standardized PSP operations

Tips: Absorb BVS did not perform standard PSP operation and increased the safty incident

The Absorb 2/3 study shows that the safty incident of TLF and stent thrombus was significantly increased and has statistical difference with metal stent due to the failure to perform PSP operation.
Sirolimus-Eluting Bioresorbable Coronary Stent Implant

 

The TLF and stent thrombus of patient using PSP and without using PSP operation in Absorb 3 study

 

Experience: Standardized PSP operation ensures safety for Neovas Stent

The application rate of PSP operation is relatively low in Absorb 2 and Absorb 3 study, the TLF and stent thrombus of BVS in three years is relatively high, displays statistical difference with metal stent; the PSP operation perform rate in Absorb China study is relatively high, the TLF and stent thrombus of BVS in three years is relatively low and has no statistical difference with metal stent.

Sirolimus-Eluting Bioresorbable Coronary Stent Implant

Comparison of stent thrombus (ST) and TLF at three years in Absorb BVS clinical study Stent thrombus (ST) and TLF at three years for NeoVas clinical study.

In Neovas clinical study, with standardized PSP operation, the TLF and ST in three years has no statistical difference. Strictly PSP operation performing is critical to significantly decrease stent adverse cardiac events.

 

Why PSP operation significantly decrease adverse cardiac events?

The direct reason of stent long-term adverse cardiac events (stent thrombus) is the stent malap- position during implantation. Stent malapposition will cause micro vascular dissection. For metal stent, stable new vessel wall will be formed after revascularization and endothelialization supported by metal stent. For bioresorbable stent, this vessel wall is unstable due to the stent degradation. Stent even breaks at thin endothelializaton tissue area and leads to the direct connection between blood and micro vascular dissection, this will cause stent thrombus rate increased higher compared with metal stent.

The objects of the regulated PSP operation is to ensure the stent apposition and exclude the vascular dissection.
Sirolimus-Eluting Bioresorbable Coronary Stent Implant

How to perform PSP operation

The critical operation flowchart of standardized PSP operation
Sirolimus-Eluting Bioresorbable Coronary Stent Implant

Ordering information
Stent Diameter
(mm)
Stent Length (mm)
12 15 18 21 24
2.75 LPS2712 LPS2715 LPS2718 LPS2721 LPS2724
3 LPS3012 LPS3015 LPS3018 LPS3021 LPS3024
3.5 LPS3512 LPS3515 LPS3518 LPS3521 LPS3524
 
Product Parameters

 

Balloon Diameter
(mm
Pressure kPa (atm)
203
(2)
405
(4)
608
(6)
709
(7)
810
(8)
1013
(10)
1216
(12)
1418
(14)
1621
(16)
1824
(18)
2027
(20)
2.75 2.6 2.66 2.71 2.73 2.75 2.82 2.88 2.94 3 3.06 3.12
3 2.84 2.89 2.95 2.97 3 3.06 3.12 3.18 3.25 3.3 3.36
3.5 3.37 3.42 3.47 3.5 3.54 3.61 3.68 3.75 3.81 3.88 3.95

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