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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_da16bb58c22a7f85e7e9050176649ab7. 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_da16bb58c22a7f85e7e9050176649ab7

Brand Name

Memo 3D ReChord Semirigid Annuloplasty Ring

Device Class

Class C

Approving Authority

CDSCO

Product Information

It is indicated for the correction of arterioventricular valve insufficiency or steno- insufficiencies

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