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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/2020/000082_aa35975f2192b4a4cfd3e160fd0bc928_d4eef93041b4f624deafbd7e766f3dd9. This device is marketed under the brand name BIOGENIX. The license holder is Biogenix Inc. 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/2020/000082_aa35975f2192b4a4cfd3e160fd0bc928_d4eef93041b4f624deafbd7e766f3dd9

Brand Name

BIOGENIX

Device Class

Class B

Approving Authority

Uttar Pradesh

Product Information

Lyse are the buffered, stabilized and micro filtered electrolyte solution for automated dilution of human blood samples, to help fully & semiautomatic analyzers to quantitative determination of erythrocytes (BIOGENIX), leukocytes (BIOGENIX) and the leukocyte subpopulations, thrombocytes (BIOGENIX) and measurement of hemoglobin (BIOGENIX) concentration

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