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Theileria Ta/To Antibody Rapid Test Kit - India CDSCO Medical Device Registration

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.

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CDSCO Registered
Class Class B
Theileria Ta/To Antibody Rapid Test Kit
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

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