Dengue Ab NS1 Rapid Test - India CDSCO Medical Device Registration

Dengue Ab NS1 Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000095_9588ed3b94673e89d5fa32583572c27a_cc92aff477bcc65afd19a68cbd64f46b. This device is marketed under the brand name Sensit Rapid. The license holder is Ubio Biotechnology Systems Private Limited, and it is classified as Device Class Class C. The approving authority is Central Drug Standard Control Organisation, South Zone.

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.

Free Database

CDSCO Registered

Class Class C

Dengue Ab NS1 Rapid Test

UID: MFG/IVD/2020/000095_9588ed3b94673e89d5fa32583572c27a_cc92aff477bcc65afd19a68cbd64f46b

Brand Name

Sensit Rapid

License Holder

Ubio Biotechnology Systems Private Limited

Device Class

Class C

Approving Authority

Central Drug Standard Control Organisation, South Zone

Product Information

Sensit Dengue Ab NS1 Rapid Test Kit is a qualitative immunochromatographic assay for the detection of IgG & IgM antibodies produced against Dengue virus in human whole blood/Serum/ Plasma. Sensit Dengue Ab NS1 Rapid Test Kit is only intended for initial screening and reactive samples should be confirmed by a supplemental assay