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Follicle Stimulating Hormone Test Kits - India CDSCO Medical Device Registration

Follicle Stimulating Hormone Test Kits is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000033_51eda08946354b16a248c5087d6342eb_8051707582ff2104d03169eaf3bb1017. The license holder is Koshbio Private Limited, and it is classified as Device Class Class B. The approving authority is Haryana.

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 Test Kits
UID: MFG/IVD/2023/000033_51eda08946354b16a248c5087d6342eb_8051707582ff2104d03169eaf3bb1017

Device Class

Class B

Approving Authority

Haryana

Product Information

A Follicle Stimulating Hormone (NA) test Kit is a medical device intended for the preliminary self testing of Follicle Stimulating Hormone (NA) in urine / body fluids

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