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Intraocular Lens - India CDSCO Medical Device Registration

Intraocular Lens is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000499_8a1919c043595ace5cab3999c55c3971_ce2f5e2a48449f56f761d14ce35874bd. This device is marketed under the brand name Clareon Vivity Extended Vision Hydrophobic IOL. The license holder is Alcon Laboratories (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
Intraocular Lens
UID: IMP/MD/2019/000499_8a1919c043595ace5cab3999c55c3971_ce2f5e2a48449f56f761d14ce35874bd

Brand Name

Clareon Vivity Extended Vision Hydrophobic IOL

Device Class

Class C

Approving Authority

CDSCO

Product Information

The Clareonโ„ข PanOptixโ„ข Trifocal IOL is indicated for primary implantation in the capsular bag in the posterior chamber of the eye for the visual correction of aphakia secondary to removal of a cataractous lens or clear lens in adult patients with and without presbyopia, who desire near, intermediate and distance vision with increased spectacle independence

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