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ISO 13485 for Inno-Spring Peripheral Stent System

Guangzhou Chenyang Package Materials Co, Ltd.
  • Type：Surgical Supplies Materials
  • Material：Nickeltitanium Wire Core
  • Ethylene Oxide Sterilization：Ethylene Oxide Sterilization
  • Quality Guarantee Period：Two Years
  • Group：Adult
  • Logo Printing：With Logo Printing

Base Info

  • Model NO.：INNO-Spring
  • Stent Model：Briad Stent
  • Catheter Size：6fr
  • Scope of Application：Lower Limb Blood Vessels
  • Application Department：Vascular Surgery Intervention
  • Certification：CE,ISO13485
  • Transport Package：Carton
  • Specification：Full Specifications
  • Trademark：INNO-SPRING
  • Origin：Suzhou China
  • HS Code：9018909919
  • Production Capacity：50000,Y

Description

 Diameter(mm)4ST-40-40ST-40-60ST-40-80ST-40-100ST-40-120ST-40-150ST-40-2004.5ST-45-40ST-45-60ST-45-80S1-45-100ST-45-120ST-45-150ST-45-2005ST-50-40ST-50-60ST-50-80ST-50-100ST-50-120ST-50-150ST-50-2005.5ST-55-40ST-55-60ST-55-80ST-55-100ST-55-120ST-55-150ST-55-2006ST-60-40ST-60-60ST-60-80ST-60-100ST-60-120ST-60-150ST-60-2006.5ST-65-40ST-65-60ST-65-80ST-65-100ST-65-120ST-65-150ST-65-2007ST-70-40ST-70-60ST-70-80ST-70-100ST-70-120ST-70-150ST-70-2007.5ST-75-40ST-75-60ST-75-80ST-75-100ST-75-120ST-75-150ST-75-2008ST-80-40ST-80-60ST-80-80ST-80-100ST-80-120ST-80-150ST-80-200
Application Range
Inno-Spring is used to treat autochthonous or occluded lesions of primary or restenosis of the superficial femoral artery and/or proximal popliteal artery up to a total length of 200 mm, with reference vessel diameters from 4 mm to 8 mm.

Product Line
ISO 13485 for Inno-Spring Peripheral Stent SystemISO 13485 for Inno-Spring Peripheral Stent SystemISO 13485 for Inno-Spring Peripheral Stent System
CertificateISO 13485 for Inno-Spring Peripheral Stent SystemISO 13485 for Inno-Spring Peripheral Stent SystemISO 13485 for Inno-Spring Peripheral Stent System