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LEPTOSPIRA ANTIBODYTEST KIT - India CDSCO Medical Device Registration

LEPTOSPIRA ANTIBODYTEST KIT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000077_a9d59245b3a0be3ca870add45f81a015_61dc165f936cf8959e6eb89203f554d3. This device is marketed under the brand name RECOMBIGEN. The license holder is RECOMBIGEN LABORATORIES PVT. LTD, and it is classified as Device Class Class B. The approving authority is North 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
LEPTOSPIRA ANTIBODYTEST KIT
UID: MFG/MD/2019/000077_a9d59245b3a0be3ca870add45f81a015_61dc165f936cf8959e6eb89203f554d3

Brand Name

RECOMBIGEN

Device Class

Class B

Approving Authority

North West Delhi Division

Product Information

Lateral flow immunoassay for the simultaneous detection of LeptospiraIgM/IgG Antibody in human serum/plasma/whole blood samples

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