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LH Rapid Quantitative Test - India CDSCO Medical Device Registration

LH Rapid Quantitative Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000278_e2155b08104291a6af4a602972eadd3d_c78c80d22e9fe68ceef8171e19e29e89. The license holder is RAPID DIAGNOSTIC 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
LH Rapid Quantitative Test
UID: IMP/IVD/2020/000278_e2155b08104291a6af4a602972eadd3d_c78c80d22e9fe68ceef8171e19e29e89

Device Class

Class B

Approving Authority

CDSCO

Product Information

Intended for quantitative determination of Luteinizing hormone ##PLACEHOLDER_0## inhuman whole blood, serum or plasma. This test is used as an aid to diagnose the ovulation cycle, premature ovarian failure and gonadal hypoplasia

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DJ Fang

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