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/2023/000617_bfce333737e58ad0b49b303b6f666645_8ff3bfb5248bec054bacc0241bd15761. This device is marketed under the brand name IntraLase Patient Interface. The license holder is Johnson & Johnson Surgical Vision 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/2023/000617_bfce333737e58ad0b49b303b6f666645_8ff3bfb5248bec054bacc0241bd15761

Brand Name

IntraLase Patient Interface

License Holder

Johnson & Johnson Surgical Vision India Pvt Ltd

Device Class

Class B

Approving Authority

CDSCO

Product Information

The IntraLase Patient Interface is designed for exclusive use with the IntraLase IFS and FS Lasers and indicated for corneal resection surgery. All components are sterile and intended for single use only.

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