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Leptospira IgM Rapid Card Kit - India CDSCO Medical Device Registration

Leptospira IgM Rapid Card Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000073_fcba8fe23d00db70832a34bbc971726d_cdca4d5adad419c59e4738965a4d349a. The license holder is Weldon Biotech India Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Uttarakhand.

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
Leptospira IgM Rapid Card Kit
UID: MFG/IVD/2023/000073_fcba8fe23d00db70832a34bbc971726d_cdca4d5adad419c59e4738965a4d349a

Device Class

Class B

Approving Authority

Uttarakhand

Product Information

Leptospira IgM Test Device is a qualitative test for the detection of IgM antibodies to Leptospira organism in human serum and plasma. The test provides a detection of anti-Leptospira IgM antibodies and can be used for the presumptive diagnosis a primary Leptospira infection. This test is for In-Vitro Diagnostic use only

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