Pure Global

Presbyopia Correcting IOL - India CDSCO Medical Device Registration

Presbyopia Correcting IOL is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000543_70184e840db45a228ecf2e7310181ae6_c5c28dc81260996603b638b43ff1b8f2. This device is marketed under the brand name Alcon Expand Series. The license holder is Alcon Laboratories (India) Pvt. Limited, 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class C
Presbyopia Correcting IOL
UID: IMP/MD/2019/000543_70184e840db45a228ecf2e7310181ae6_c5c28dc81260996603b638b43ff1b8f2

Brand Name

Alcon Expand Series

Device Class

Class C

Approving Authority

CDSCO

Product Information

The AcrySof IQ PanOptix Toric Presbyopia-Correcting intraocular lens is intended for primary implantation in the capsular bag in the posterior chamber of the human eye for the visual correction of aphakia and pre-existing corneal astigmatism 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

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing