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Chikungunya Antibody test - India CDSCO Medical Device Registration

Chikungunya Antibody test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000107_1aa55ff929d4f386b2b8d923e91d49ab_e5af97ccf4b8bb12441e855bfbaeef2b. 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
Chikungunya Antibody test
UID: MFG/IVD/2020/000107_1aa55ff929d4f386b2b8d923e91d49ab_e5af97ccf4b8bb12441e855bfbaeef2b

Brand Name

human Chorionic Gonadotropin

Device Class

Class B

Approving Authority

Rajasthan

Product Information

Chikungunya test is an in vitro diagnostic rapid test based on the principle of immunochromatography on a membrane, for simultaneous and differential detection of Chikungunya specific antibody (human Chorionic Gonadotropin) in human serum / plasma / WB for diagnosis of Chikungunya infection

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DJ Fang

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