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/2018/000001_aa35975f2192b4a4cfd3e160fd0bc928_76a67554b98d1b25472d18c243de7233. This device is marketed under the brand name LiquiMAX, Lyphomax, Automax and other OEM Brands. The license holder is Avecon Healthcare Pvt. Ltd, and it is classified as Device Class Class B. The approving authority is Haryana.

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.

Free Database

CDSCO Registered

Class Class B

Lyse Reagent

UID: MFG/IVD/2018/000001_aa35975f2192b4a4cfd3e160fd0bc928_76a67554b98d1b25472d18c243de7233

Brand Name

LiquiMAX, Lyphomax, Automax and other OEM Brands

License Holder

Avecon Healthcare Pvt. Ltd

Device Class

Class B

Approving Authority

Haryana

Product Information

CF-Lyse-Diff is used for hematological analysis by the hematological analyzer as a red blood cell hemolysing reagent for the assay of white blood cell count, lymphocytes count, and granulocyte count