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Salmonella typhi IgG &IgM Test/device - India CDSCO Medical Device Registration

Salmonella typhi IgG &IgM Test/device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000107_9a9c1c38ae9ea471e277a2c3cbbadee3_54d31e08c4dd070532e9096c71349c1a. This device is marketed under the brand name human Chorionic Gonadotropin. The license holder is M/s ASTAM DIAGNOSTICS PVT. LTD., and it is classified as Device Class Class B. The approving authority is Rajasthan.

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
Salmonella typhi IgG &IgM Test/device
UID: MFG/IVD/2020/000107_9a9c1c38ae9ea471e277a2c3cbbadee3_54d31e08c4dd070532e9096c71349c1a

Brand Name

human Chorionic Gonadotropin

Device Class

Class B

Approving Authority

Rajasthan

Product Information

for detection of S.typhi (human Chorionic Gonadotropin) in human serum/ Plasma/ whole blood

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