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Kala Azar Antibody Test Device - India CDSCO Medical Device Registration

Kala Azar Antibody Test Device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000107_d3d06c74e1c46123550e0dea9f6660be_d259c6fdda9a8d00cf94c6bb73ad4b62. 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
Kala Azar Antibody Test Device
UID: MFG/IVD/2020/000107_d3d06c74e1c46123550e0dea9f6660be_d259c6fdda9a8d00cf94c6bb73ad4b62

Brand Name

human Chorionic Gonadotropin

Device Class

Class B

Approving Authority

Rajasthan

Product Information

Kala azar Antibody Test Device is a rapid, qualitative, two site sandwich immunoassay for the determination of antibodies to Visceral Leishmaniasis (human Chorionic Gonadotropin), members of L. donovani, in human serum / plasma / whole blood specimens. For professional use only

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