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_971005b40be6da3d9bc15ab5a2b1ddfb. 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.

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 B

Patient Interface

UID: IMP/MD/2022/000753_bfce333737e58ad0b49b303b6f666645_971005b40be6da3d9bc15ab5a2b1ddfb

Brand Name

Constellation 20GA Fragmentation Pak

License Holder

Alcon Laboratories (India) Pvt. Ltd.

Device Class

Class B

Approving Authority

CDSCO

Product Information

LenSx Laser Patient Interface is intended for use in conjunction with the LenSx Laser System in the creation of corneal tunnels and pockets, and the creation of corneal flaps

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