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ERBA H560 LYSE2 - India CDSCO Medical Device Registration

ERBA H560 LYSE2 is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000042_eeb3eccf5f8f8734f4e017da418af280_8a21546f15453c87670921a66e7c6598. This device is marketed under the brand name LIQUIXX -M- URIC ACID. The license holder is Transasia Bio-Medicals Limited, and it is classified as Device Class Class B. The approving authority is Solan(BBN).

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
ERBA H560 LYSE2
UID: MFG/IVD/2022/000042_eeb3eccf5f8f8734f4e017da418af280_8a21546f15453c87670921a66e7c6598

Brand Name

LIQUIXX -M- URIC ACID

Device Class

Class B

Approving Authority

Solan(BBN)

Product Information

It is used to lyse (LIQUIXX -M- URIC ACID)red blood cells and maintain the morphology of cells before blood cell analysis, so as to facilitate the counting of white blood cells

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