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CDSCO UID IMP/MD/2023/000617_bfce333737e58ad0b49b303b6f666645_8ff3bfb5248bec054bacc0241bd15761

Patient Interface

Johnson & Johnson Surgical Vision India Pvt Ltd·Device Class Class B·India CDSCO·Brand: IntraLase Patient Interface
Registration details
UID
IMP/MD/2023/000617_bfce333737e58ad0b49b303b6f666645_8ff3bfb5248bec054bacc0241bd15761
Device class
Class B
Brand name
IntraLase Patient Interface
License holder
Johnson & Johnson Surgical Vision India Pvt Ltd
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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About this record

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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