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Lyse reagent - India CDSCO Medical Device Registration

Lyse reagent is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000088_d07d2ad237c25d66b17784c668495de7_75b3677387009717ed9e84eafa1e85f3. This device is marketed under the brand name HaemNest Sheath Fluid. The license holder is Genenest Biotech Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Uttar Pradesh.

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.

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CDSCO Registered
Class Class B
Lyse reagent
UID: MFG/IVD/2022/000088_d07d2ad237c25d66b17784c668495de7_75b3677387009717ed9e84eafa1e85f3

Brand Name

HaemNest Sheath Fluid

Device Class

Class B

Approving Authority

Uttar Pradesh

Product Information

For cell classification count or hemoglobin quantitative measurement

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