Patient Interface - India CDSCO Medical Device Registration

Patient Interface is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2022/000753_bfce333737e58ad0b49b303b6f666645_937a310d5468cea35193c2ef67c1f0df. This device is marketed under the brand name Constellation 20GA Fragmentation Pak. The license holder is Alcon Laboratories (India) Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is CDSCO.

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CDSCO Registered

Class Class B

Patient Interface

UID: IMP/MD/2022/000753_bfce333737e58ad0b49b303b6f666645_937a310d5468cea35193c2ef67c1f0df

Brand Name

Constellation 20GA Fragmentation Pak

License Holder

Alcon Laboratories (India) Pvt. Ltd.

Device Class

Class B

Approving Authority

CDSCO

Product Information

LenSx Laser SoftFit Patient Interface is intended for use in conjunction with the LenSx Laser System in cataract surgery including anterior capsulotomy, phacofragmentation, and the creation of a single plane and multi-plane arc cuts/incisions in the cornea, each of which may be performed either individually or consecutively during the same procedure

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