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Annuloplasty Device - India CDSCO Medical Device Registration

Annuloplasty Device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000392_2f94374abd14ee777b52bfec9c00c5c3_2169457a44f9f7a8ce30703b0d1b0da3. This device is marketed under the brand name Memo 3D ReChord Semirigid Annuloplasty Ring. The license holder is LIVANOVA INDIA 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.

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CDSCO Registered
Class Class C
Annuloplasty Device
UID: IMP/MD/2018/000392_2f94374abd14ee777b52bfec9c00c5c3_2169457a44f9f7a8ce30703b0d1b0da3

Brand Name

Memo 3D ReChord Semirigid Annuloplasty Ring

Device Class

Class C

Approving Authority

CDSCO

Product Information

It is used for correction of congenital or acquired mitral insufficiencies with dilation and deformation of the mitral annulus

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