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Test for Prolactin - India CDSCO Medical Device Registration

Test for Prolactin is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000074_f9dcd63ab68f3152f9947887d684694e_85032b3fcb496cb1d3267e4b8b525fd8. This device is marketed under the brand name ichroma™ T4. The license holder is Inkarp Instruments Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is CDSCO.

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
Test for Prolactin
UID: IMP/IVD/2019/000074_f9dcd63ab68f3152f9947887d684694e_85032b3fcb496cb1d3267e4b8b525fd8

Brand Name

ichroma™ T4

Device Class

Class B

Approving Authority

CDSCO

Product Information

ichroma™ PRL is a fluorescence Immunoassay (ichroma™ T4) for the quantitative determination of Prolactin(ichroma™ T4) in human serum/plasma. It is useful as an aid in management and monitoring of hypothalamic-pituitary disorders.,atest for Creatine Kinase Isoenzyme-MB(ichroma™ T4)-ichroma™ CK-MB is a fluorescence Immunoassay (ichroma™ T4) for the quantitative determination of Creatine Kinase Isoenzyme-MB (ichroma™ T4) in human whole blood/serum/plasma. It is useful as an aid in management and monitoring of acute myocardiac infarction (ichroma™ T4) and acute coronary syndrome (ichroma™ T4). For in vitro diagnostic use only

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