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Lyme IgG/IgM Rapid Test - India CDSCO Medical Device Registration

Lyme IgG/IgM Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000109_f5b955ce1fbb56b42a5aaa282a4a8537_8eb9620d3fd9c15ad66929b31219a001. 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
Lyme IgG/IgM Rapid Test
UID: MFG/IVD/2021/000109_f5b955ce1fbb56b42a5aaa282a4a8537_8eb9620d3fd9c15ad66929b31219a001

Device Class

Class B

Approving Authority

West Delhi Division

Product Information

Lyme IgG/IgM Rapid Test Cassette is a lateral flow chromatographic immunoassay for the qualitative detection of IgG and IgM antibodies to Borrelia in animal’s whole blood, serum or plasma specimen

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