Test for Progesterone - India CDSCO Medical Device Registration

Test for Progesterone is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000203_1c41e697f9be20f3acbfac837d0a9720_b58a8fbc36f8a4cad1c86cc6721094eb. 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.

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CDSCO Registered

Class Class B

Test for Progesterone

UID: IMP/MD/2018/000203_1c41e697f9be20f3acbfac837d0a9720_b58a8fbc36f8a4cad1c86cc6721094eb

Brand Name

QDx Instacheck™ Cortisol

License Holder

DiaSys Diagnostics India Private Limited

Device Class

Class B

Approving Authority

CDSCO

Product Information

QDx Instacheck™ Progesterone along with QDx Instacheck™ Reader is a fluorescence Immunoassay (QDx Instacheck™ Cortisol) for the quantitative determination of progesterone in human serum/plasma. It is useful as an aid in management and monitoring of the cause of infertility, track ovulation, diagnose an ectopic or failing pregnancy, monitor the health of a pregnancy

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Test for total 25 D2/D3

Brand: QDx Instacheck™ Cortisol

DiaSys Diagnostics India Private Limited

Test for Progesterone - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

DJ Fang

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