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ERBAQIK Dengue duo - India CDSCO Medical Device Registration

ERBAQIK Dengue duo is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000014_3fdee5d33aa08cfd31c999e892cebb9b_5b1ecdad7b864fad13f7b5a2285195d4. This device is marketed under the brand name ERBAQIK Dengue Alpha NS1Ag. The license holder is M/s.Transasia Bio-Medicals Ltd., and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, West 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.

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CDSCO Registered
Class Class C
ERBAQIK Dengue duo
UID: MFG/IVD/2020/000014_3fdee5d33aa08cfd31c999e892cebb9b_5b1ecdad7b864fad13f7b5a2285195d4

Brand Name

ERBAQIK Dengue Alpha NS1Ag

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

Detection of both Dengue virus NS1 antigen and IgG/IgM antibodies to dengue virus in human serum, plasma or whole blood

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