Pure Global
CDSCO UID MFG/MD/2019/000060_06fae7f90fd21651bb1906c522a76612_b81ded89cfa152baa4d869986a1c2bbb

Hydrophilic Acrylic Foldable IOL

Omni Lens Pvt. Ltd·Device Class Class C·India CDSCO·Brand: OMNI, Intra,C-Thru, Innova,Innova plus,BIOL,Techno Instrument Lens,.Acrivue,GenNext, Revive, Axis
Registration details
UID
MFG/MD/2019/000060_06fae7f90fd21651bb1906c522a76612_b81ded89cfa152baa4d869986a1c2bbb
Device class
Class C
Brand name
OMNI, Intra,C-Thru, Innova,Innova plus,BIOL,Techno Instrument Lens,.Acrivue,GenNext, Revive, Axis
License holder
Omni Lens Pvt. Ltd
Approving authority
Central Drug Standards Control Organization, Ahmedabad
Product information
Intra Ocular Lens is used for replacing natural eye lens in the ophthalmic region by surgical incision in the eye
Similar products (2)
Other products with the same name or brand
PMMA Intra Ocular Lens
Brand: OMNI, Intra,C-Thru, Innova,Innova plus,BIOL,Techno Instrument Lens,.Acrivue,GenNext, Revive, Axis
Omni Lens Pvt. Ltd
Class C
Hydrophobic Acrylic Foldable IOL
Brand: OMNI, Intra,C-Thru, Innova,Innova plus,BIOL,Techno Instrument Lens,.Acrivue,GenNext, Revive, Axis
Omni Lens Pvt. Ltd
Class C
Other products from Omni Lens Pvt. Ltd
Products from the same license holder (6 products)
Cartridge
Class B
Cushion
Class A
Lens Delivery System
Class B
PMMA Intra Ocular Lens
Brand: OMNI, Intra,C-Thru, Innova,Innova plus,BIOL,Techno Instrument Lens,.Acrivue,GenNext, Revive, Axis
Class C
Capsular Tension Ring
Class C
Hydrophobic Acrylic Foldable IOL
Brand: OMNI, Intra,C-Thru, Innova,Innova plus,BIOL,Techno Instrument Lens,.Acrivue,GenNext, Revive, Axis
Class C
About this record

Hydrophilic Acrylic Foldable IOL is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000060_06fae7f90fd21651bb1906c522a76612_b81ded89cfa152baa4d869986a1c2bbb. This device is marketed under the brand name OMNI, Intra,C-Thru, Innova,Innova plus,BIOL,Techno Instrument Lens,.Acrivue,GenNext, Revive, Axis. The license holder is Omni Lens Pvt. Ltd, and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, Ahmedabad.

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.