Follicle Stimulating Hormone Rapid Test(BIOGENIX ) - India CDSCO Medical Device Registration

Follicle Stimulating Hormone Rapid Test(BIOGENIX ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000082_f3adc7a19487fb7e0d789bb92f49a9e4_c02f727d1458621f848b91a6e8379362. This device is marketed under the brand name BIOGENIX. The license holder is Biogenix Inc. Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Uttar Pradesh.

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CDSCO Registered

Class Class B

Follicle Stimulating Hormone Rapid Test(BIOGENIX )

UID: MFG/IVD/2020/000082_f3adc7a19487fb7e0d789bb92f49a9e4_c02f727d1458621f848b91a6e8379362

Brand Name

BIOGENIX

License Holder

Biogenix Inc. Pvt. Ltd.

Device Class

Class B

Approving Authority

Uttar Pradesh

Product Information

The FSH One Step Menopause Rapid Test Device (BIOGENIX) is a rapid chromatographic immunoassay for the qualitative detection of Follicle-stimulating hormone (BIOGENIX) level in urine to evaluate the onset of menopause in women

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FT3 CLIA Test Reagent Kit

Brand: BIOGENIX

Biogenix Inc. Pvt. Ltd.

Follicle Stimulating Hormone Rapid Test(BIOGENIX ) - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

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