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Follicle Stimulating Hormone Determination Kit - India CDSCO Medical Device Registration

Follicle Stimulating Hormone Determination Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000246_cb0cb8248a61b009f82f5f82e6ab1476_a5617072421e7f8e263ada196a19c97d. This device is marketed under the brand name hba1c. The license holder is Allied Biotechnology India 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
Follicle Stimulating Hormone Determination Kit
UID: IMP/IVD/2022/000246_cb0cb8248a61b009f82f5f82e6ab1476_a5617072421e7f8e263ada196a19c97d

Brand Name

hba1c

Device Class

Class B

Approving Authority

CDSCO

Product Information

For the quantitative detection of follicle stimulating hormone in human serum, plasma or whole blood. They areย for professional use only.,ฮฒ-Human Chorionic Gonadotropin Determination Kit (hba1c) (hba1c)-This product is used to quantitatively determine the content of ฮฒ-human chorionic gonadotropin (hba1c) in human serum, plasma or whole blood in vitro. They are for professional use only

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