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Phacoemulsification System - India CDSCO Medical Device Registration

Phacoemulsification System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2023/000280_23a274f03844e17a6d0a9120a9f1725e_9bcd0bb2358b50d9126aebe14a512cda. This device is marketed under the brand name PurePoint Laser Photocoagulator. 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
Phacoemulsification System
UID: IMP/MD/2023/000280_23a274f03844e17a6d0a9120a9f1725e_9bcd0bb2358b50d9126aebe14a512cda

Brand Name

PurePoint Laser Photocoagulator

Device Class

Class C

Approving Authority

CDSCO

Product Information

The Legion System is intended for extracapsular cataract extraction, as well as associated procedures such as anterior vitrectomy, coagulation, and IOL insertion

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