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Lyse LB (HaemNest Lyse LB ) - India CDSCO Medical Device Registration

Lyse LB (HaemNest Lyse LB ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000088_f0ef82184f8d25f723deb092fcf7376e_60e5f9434cc188ac1e745fea92cecca4. 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 LB (HaemNest Lyse LB )
UID: MFG/IVD/2022/000088_f0ef82184f8d25f723deb092fcf7376e_60e5f9434cc188ac1e745fea92cecca4

Brand Name

HaemNest Sheath Fluid

Device Class

Class B

Approving Authority

Uttar Pradesh

Product Information

For all classification count or hemoglobin quantitative measurement

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