EbraQik COVID-19 Rapid Antigen Test - India CDSCO Medical Device Registration

EbraQik COVID-19 Rapid Antigen Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000014_a78e4b7b08890518c34050881b63862d_56ca4908dd1ad81fddffba3a108b1ed0. 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.

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CDSCO Registered

Class Class C

EbraQik COVID-19 Rapid Antigen Test

UID: MFG/IVD/2020/000014_a78e4b7b08890518c34050881b63862d_56ca4908dd1ad81fddffba3a108b1ed0

Brand Name

ERBAQIK Dengue Alpha NS1Ag

License Holder

M/s.Transasia Bio-Medicals Ltd.

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

ErbaQik COVID-19 Ag test is intended for self-testing at home for the detection of COVID-19 Antigen in human Nasopharyngeal Sample. This test is authorized and intended for non-prescription home use as self-test with the self-collected nasal specimens from individuals of age 18 years or older & with adult collected nasal specimen from individuals aged 2 years or older. The report is provided by ErbaQik App (ERBAQIK Dengue Alpha NS1Ag) and the results can be interpreted by the user

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ERBAQIK Dengue IgG/IgM

Brand: ERBAQIK Dengue Alpha NS1Ag

M/s.Transasia Bio-Medicals Ltd.

EbraQik COVID-19 Rapid Antigen Test - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

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