CDSCO UID MFG/MD/2019/000008_6fe54519b39bd65e1cbb3277b234f344_29a838d528b5e8cccd9e594da3d7816b

Polymer free Hydroxyapatite coated Sirolimus Eluting Coronary Stent System

PURPLE MICROPORT CARDIOVASCULAR PRIVATE LIMITED·Device Class Class D·India CDSCO·Brand: Vestasync Sirolimus Eluting Coronary Stent System
Registration details
UID
MFG/MD/2019/000008_6fe54519b39bd65e1cbb3277b234f344_29a838d528b5e8cccd9e594da3d7816b
Device class
Class D
Brand name
Vestasync Sirolimus Eluting Coronary Stent System
Approving authority
Central Drug Standards Control Organization, Ahmedabad
Product information
Product is indicated for improving coronary luminal diameter in patients with symptomatic ischemic heart disease in de novo coronary artery lesion in native coronary arteries in patients eligible for percutaneous Transluminal Coronary Angioplasty (Vestasync Sirolimus Eluting Coronary Stent System)
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About this record

Polymer free Hydroxyapatite coated Sirolimus Eluting Coronary Stent System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000008_6fe54519b39bd65e1cbb3277b234f344_29a838d528b5e8cccd9e594da3d7816b. This device is marketed under the brand name Vestasync Sirolimus Eluting Coronary Stent System. The license holder is PURPLE MICROPORT CARDIOVASCULAR PRIVATE LIMITED, and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, Ahmedabad.

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