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HAV IgM Rapid Test - India CDSCO Medical Device Registration

HAV IgM Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000109_f0c8e247aa7de545890a48f59be360de_69a451a9a81ddb300f0fbdf3069cf414. The license holder is Biotrol Laboratories Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is West Delhi Division.

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
HAV IgM Rapid Test
UID: MFG/IVD/2021/000109_f0c8e247aa7de545890a48f59be360de_69a451a9a81ddb300f0fbdf3069cf414

Device Class

Class B

Approving Authority

West Delhi Division

Product Information

HAV IgM Rapid Test is a rapid chromatographic immunoassay for the qualitative detection of IgM antibody to Hepatitis A Virus ##PLACEHOLDER_0## in serum, plasma & Whole Blood

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