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Multi-fenestrated ASD Occluder - India CDSCO Medical Device Registration

Multi-fenestrated ASD Occluder is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000404_c4f1fd365be6275034f8a3dca4fa523e_bbc8fe2cced341e33c231fdfca45ee26. 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
Multi-fenestrated ASD Occluder
UID: IMP/MD/2018/000404_c4f1fd365be6275034f8a3dca4fa523e_bbc8fe2cced341e33c231fdfca45ee26

Brand Name

ASD

Device Class

Class D

Approving Authority

CDSCO

Product Information

The CeraTM Multi-Fenestrated ASD Occluder is a percutaneous, transcatheter, atrial septal defect closure device intended for the occlusion of multi-fenestrated atrial septal defects (ASD)

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