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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/2022/000101_2f94374abd14ee777b52bfec9c00c5c3_e32ce1b09493c39dc4220bf23cfc0505. This device is marketed under the brand name Sovering Annuloplasty Device. The license holder is Parekh Integrated Services 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/2022/000101_2f94374abd14ee777b52bfec9c00c5c3_e32ce1b09493c39dc4220bf23cfc0505

Brand Name

Sovering Annuloplasty Device

Device Class

Class C

Approving Authority

CDSCO

Product Information

Memo 4D device is intended to reshape and support the mitral annulus after the surgical repair. The decision to undertake a mitral valve repair must remain with the surgeon after having evaluated short- and long-terms risks and benefits towards alternative procedures and on the visual inspection of the lesion in the individual case

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