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Test for Luteinizing hormone - India CDSCO Medical Device Registration

Test for Luteinizing hormone is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000203_9a702b5ab814b0f556015538b5b1038a_9ea3b6a74be76071d232997a24d92237. This device is marketed under the brand name QDx Instacheck™ Cortisol. The license holder is DiaSys Diagnostics India Private Limited, 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 Luteinizing hormone
UID: IMP/MD/2018/000203_9a702b5ab814b0f556015538b5b1038a_9ea3b6a74be76071d232997a24d92237

Brand Name

QDx Instacheck™ Cortisol

Device Class

Class B

Approving Authority

CDSCO

Product Information

QDx Instacheck™ LH along with QDx Instacheck™ Reader is a fluorescence immunoassay that quantifies concentration of Luteinizing hormone (QDx Instacheck™ Cortisol) in human serum/plasma. It is useful as an aid in management and monitoring of determination of evaluating fertility issues, function of reproductive organs (QDx Instacheck™ Cortisol), or detection of the ovulation

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