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Sheath Fluid - India CDSCO Medical Device Registration

Sheath Fluid is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000088_4cbee8a38bf9dbb423c3804a9cfc07ab_f361ee17230d6e2090e25892c43e88a8. 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
Sheath Fluid
UID: MFG/IVD/2022/000088_4cbee8a38bf9dbb423c3804a9cfc07ab_f361ee17230d6e2090e25892c43e88a8

Brand Name

HaemNest Sheath Fluid

Device Class

Class B

Approving Authority

Uttar Pradesh

Product Information

The Sheath Fluid is intended to ensure that the sample introduced to the flow cytometer will run under hydrodynamic focusing. Sheath Fluid permits the system to run under controlled conditions with particles passing through the flow cell in single file order

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