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Bovine Anaplasma Antibody Rapid Test - India CDSCO Medical Device Registration

Bovine Anaplasma Antibody Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000022_e4e4de7e4af75730dcbaf4ce874a17ea_0b7238b19f5cd5ea4ca20af4cc94be7b. This device is marketed under the brand name Sensit. The license holder is Ubio Biotechnology Systems Private Limited, and it is classified as Device Class Class B. The approving authority is Kerala.

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
Bovine Anaplasma Antibody Rapid Test
UID: MFG/IVD/2020/000022_e4e4de7e4af75730dcbaf4ce874a17ea_0b7238b19f5cd5ea4ca20af4cc94be7b

Brand Name

Sensit

Device Class

Class B

Approving Authority

Kerala

Product Information

quickVET Bovine Anaplasma Antibody Rapid Test is a qualitative immunochromatographic assay for the detection Anaplasma antibodies in Bovine whole blood, plasma or serum

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