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PDA [Patent Ductus Arteriosus] Occluder - India CDSCO Medical Device Registration

PDA [Patent Ductus Arteriosus] Occluder is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000404_e49f4b4263139549419544a32ebfc9b4_8584a780e24beee3265bb4ca19aed858. 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
PDA [Patent Ductus Arteriosus] Occluder
UID: IMP/MD/2018/000404_e49f4b4263139549419544a32ebfc9b4_8584a780e24beee3265bb4ca19aed858

Brand Name

ASD

Device Class

Class D

Approving Authority

CDSCO

Product Information

The HeartRTM PDA Occluder is a percutaneous, transcatheter device, intended for the non-surgical closure of patent ductus arteriosus (ASD)

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