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LIPASE - India CDSCO Medical Device Registration

LIPASE is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000042_da420ad455b311de7240696d109fe287_986073644190a3b9a3462639faf6fa5e. 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
LIPASE
UID: MFG/IVD/2022/000042_da420ad455b311de7240696d109fe287_986073644190a3b9a3462639faf6fa5e

Brand Name

LIQUIXX -M- URIC ACID

Device Class

Class B

Approving Authority

Solan(BBN)

Product Information

Diagnostic reagent for quantitative in vitro determination of LIPASE in human serum and plasma

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