CDSCO UID MFG/IVD/2020/000060_fbad0ffcc06c50c3b1a464f630203bd4_fcea163b1aa2e9c2071ce51905bce43d

Theileria Ta/To Antibody Rapid Test Kit

Genomix Molecular Diagnostics Pvt Ltd·Device Class Class B·India CDSCO
Registration details
UID
MFG/IVD/2020/000060_fbad0ffcc06c50c3b1a464f630203bd4_fcea163b1aa2e9c2071ce51905bce43d
Device class
Class B
Approving authority
Telangana
Product information
For in vitro detection of Theileria antibodies in plasma or serum
Other products from Genomix Molecular Diagnostics Pvt Ltd
Products from the same license holder (10 products)
Bovine Leptospira Antibody indirect ELISA test Kit
Class B
Rhodococcus Antibody Rapid Test Kit
Class B
Classical Swine Fever Antibody Rapid Test Kit
Class B
Leptospira Antibody ELISA Test Kit
Class B
EIA Antibody Rapid Test Kit
Class B
Campylobacter Antibody Rapid Test Kit
Class B
Glanders Antibody detection Rapid Test Kit
Class B
Chikungunya virus IgM Antibody ELISA test Kit
Class B
Anti-Mullerian Hormone ELISA test Kit
Brand: EIA
Class B
IBR Antibody Rapid Test Kit
Class B
About this record

Theileria Ta/To Antibody Rapid Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000060_fbad0ffcc06c50c3b1a464f630203bd4_fcea163b1aa2e9c2071ce51905bce43d. The license holder is Genomix Molecular Diagnostics Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Telangana.

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.