ADENOSINE DEAMINASE - India CDSCO Medical Device Registration

ADENOSINE DEAMINASE is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000042_9454bd9d75396b36af478b2c0700703c_2893481664895dd5e524f4718cbe65ba. 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.

Free Database

CDSCO Registered

Class Class B

ADENOSINE DEAMINASE

UID: MFG/IVD/2022/000042_9454bd9d75396b36af478b2c0700703c_2893481664895dd5e524f4718cbe65ba

Brand Name

LIQUIXX -M- URIC ACID

License Holder

Transasia Bio-Medicals Limited

Device Class

Class B

Approving Authority

Solan(BBN)

Product Information

Diagnostic reagent for quantitative in vitro determination of ADA in human serum and plasma. Adenosine Deaminase (LIQUIXX -M- URIC ACID) Assay Kit is for determination of ADA activity in Serum, Plasma, Pleural fluid and Cerebrospinal fluid samples