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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_f03297ca41c2d0f5e593ea8d64026196. 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_f03297ca41c2d0f5e593ea8d64026196

Brand Name

Sovering Annuloplasty Device

Device Class

Class C

Approving Authority

CDSCO

Product Information

Sovering annuloplasty device is indicated to support the mitral or the tricuspid annulus after the surgical repair. The decision on whether or not to undertake valvuloplasty can be made only by the surgeon for each individual case, on the basis of an assessment of the prospective short and medium-term risks/benefits compared to alternative treatment methods

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