Sodium Hyaluronate 3% w/v with Chondroitin sulphate 4% w/v ophthalmic solution for Domestic and Export purpose - India CDSCO Medical Device Registration

Sodium Hyaluronate 3% w/v with Chondroitin sulphate 4% w/v ophthalmic solution for Domestic and Export purpose is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000225_eb8fdb64b24df48360d902d7b73f3166_d3843c2cee9e94c239c50fbc83a3d7ed. This device is marketed under the brand name -----. The license holder is AUROLAB, and it is classified as Device Class Class C. The approving authority is Central Drug Standard Control Organisation, South Zone.

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CDSCO Registered

Class Class C

Sodium Hyaluronate 3% w/v with Chondroitin sulphate 4% w/v ophthalmic solution for Domestic and Export purpose

UID: MFG/MD/2019/000225_eb8fdb64b24df48360d902d7b73f3166_d3843c2cee9e94c239c50fbc83a3d7ed

Brand Name

-----

License Holder

AUROLAB

Device Class

Class C

Approving Authority

Central Drug Standard Control Organisation, South Zone

Product Information

The medical device is indicated as surgical adjunct during surgical procedures involving the anterior chamber of the eye, including cataract extraction and insertion of intraocular lenses. It maintains the depth of the anterior chamber during the whole surgical procedure and permits greater operative precision without the risk of damaging the endothelium of the cornea or other intraocular tissues

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Sodium Hyaluronate Ophthalmic Solution 1.4% w/v for Domestic and Export pupose

Brand: -----

AUROLAB

Sodium Hyaluronate 3% w/v with Chondroitin sulphate 4% w/v ophthalmic solution for Domestic and Export purpose - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

DJ Fang

Sodium Hyaluronate Ophthalmic Solution 1.4% w/v for Domestic and Export pupose

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