Test for Follicle stimulating hormone - India CDSCO Medical Device Registration

Test for Follicle stimulating hormone is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000203_f35a92f69beaa3354496fcc2530b8f6e_7659e5ee3b82286156db74a72f49687f. 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 Follicle stimulating hormone

UID: IMP/MD/2018/000203_f35a92f69beaa3354496fcc2530b8f6e_7659e5ee3b82286156db74a72f49687f

Brand Name

QDx Instacheck™ Cortisol

License Holder

DiaSys Diagnostics India Private Limited

Device Class

Class B

Approving Authority

CDSCO

Product Information

QDx Instacheck™ FSH in conjunction with QDx Instacheck™ Reader is a fluorescence immunoassay for quantitative measurement of follicle stimulating hormone (QDx Instacheck™ Cortisol) in human serum/plasma. It is useful as an aid in management and monitoring of concentration of FSH

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Test for total 25 D2/D3

Brand: QDx Instacheck™ Cortisol

DiaSys Diagnostics India Private Limited

Test for Follicle stimulating hormone - India CDSCO Medical Device Registration

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Device Class

Approving Authority

Product Information

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