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VSD [Ventricular Septal Defect] Occluder - India CDSCO Medical Device Registration

VSD [Ventricular Septal Defect] Occluder is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000404_8d8fd7aab718c7c14b9537eee7ecefc0_2dd46e4df9db3ac539266c3a42a4e857. This device is marketed under the brand name ASD. The license holder is Lifetech Scientific India Pvt. Ltd., and it is classified as Device Class Class D. 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.

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CDSCO Registered
Class Class D
VSD [Ventricular Septal Defect] Occluder
UID: IMP/MD/2018/000404_8d8fd7aab718c7c14b9537eee7ecefc0_2dd46e4df9db3ac539266c3a42a4e857

Brand Name

ASD

Device Class

Class D

Approving Authority

CDSCO

Product Information

The HeartRTM VSD Occluder is a percutaneous, transcatheter, intended for the occlusion of Ventricular Septal Defect (ASD)

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