Kala Azar Antibody Test Device
- UID
- MFG/IVD/2020/000107_d3d06c74e1c46123550e0dea9f6660be_d259c6fdda9a8d00cf94c6bb73ad4b62
- Device class
- Class B
- Brand name
- human Chorionic Gonadotropin
- License holder
- M/s ASTAM DIAGNOSTICS PVT. LTD.
- 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
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.