Ophthalmic laser Probe(Laser Probe )
- UID
- IMP/MD/2023/000280_5d6e0ba49edd067e58b9d9970e61733a_744d77479a5026296ca9cd8bf1dd008c
- Device class
- Class C
- Brand name
- PurePoint Laser Photocoagulator
- License holder
- Alcon Laboratories (India) Pvt. Ltd.
- Approving authority
- CDSCO
- Product information
- The Alcon laser probes are used for transmission of laser energy to the eye, to reattach the retina, and to remove new vascularization resulting from conditions such as diabetes, macular degeneration and glaucoma. In addition, the laser probes are also used for the following treatments and conditions: Retinal photocoagulation, panretinal photocoagulation and intravitreal photocoagulation of vascular and structural abnormalities of the retina and choroid including: • Proliferative and nonproliferative retinopathy (PurePoint Laser Photocoagulator) • Choroidal neovascularization secondary to age-related macular degeneration • Retinal tears and detachments • Macular edema • Retinopathy of prematurity • Choroidal neovascularization • Leaking micro-aneurysmsIridotomy/ Iridectomy for treatment of Chronic/Primary Open Angle Glaucoma (PurePoint Laser Photocoagulator) and Refractory Glaucoma. Trabeculoplasty for treatment of Chronic/Primary Open Angle Glaucoma (PurePoint Laser Photocoagulator) and refractory Glaucoma. And other laser treatments including: • Internal sclerostomy • Lattice degeneration • Central and Branch Retinal Vein Occlusion • Suturelysis • Vascular and pigmented skin lesions
Ophthalmic laser Probe(Laser Probe ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2023/000280_5d6e0ba49edd067e58b9d9970e61733a_744d77479a5026296ca9cd8bf1dd008c. This device is marketed under the brand name PurePoint Laser Photocoagulator. The license holder is Alcon Laboratories (India) Pvt. Ltd., and it is classified as Device Class Class C. The approving authority is CDSCO.
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