Stent Graft System - India CDSCO Medical Device Registration

Stent Graft System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000466_4e1501c99ce27b28129b025c3e7fdcf9_f5e8e88819b1ab15068778fa3f6df800. This device is marketed under the brand name BeGraft Peripheral. The license holder is Vibgyor Health Care Pvt. Ltd., and it is classified as Device Class Class C. The approving authority is CDSCO.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

Free Database

CDSCO Registered

Class Class C

Stent Graft System

UID: IMP/MD/2019/000466_4e1501c99ce27b28129b025c3e7fdcf9_f5e8e88819b1ab15068778fa3f6df800

Brand Name

BeGraft Peripheral

License Holder

Vibgyor Health Care Pvt. Ltd.

Device Class

Class C

Approving Authority

CDSCO

Product Information

The BeGraft Peripheral Stent Graft System is indicated for intraluminal chronic placement in iliac and renal arteries for: • Restoring and improving the patency and • Treating aneurysms, acute perforations, acute ruptures and fistulas.

Class D

Brand: E-vita Thoracic 3G

Class D