Standard Q COVID-19 IgM/IgG DUO - India CDSCO Medical Device Registration

Standard Q COVID-19 IgM/IgG DUO is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2018/000005_a05040b4504d6074780d32063eb1a597_8ae3bede8be31870660ec9b6eb2b7ecb. This device is marketed under the brand name STANDARD Q Dengue NS1 Ag Test, ULTRA Dengue NS1 Ag Test. The license holder is SD Biosensor Healthcare Pvt. Ltd, and it is classified as Device Class Class C. The approving authority is Sub Zonal Baddi.

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CDSCO Registered

Class Class C

Standard Q COVID-19 IgM/IgG DUO

UID: MFG/MD/2018/000005_a05040b4504d6074780d32063eb1a597_8ae3bede8be31870660ec9b6eb2b7ecb

Brand Name

STANDARD Q Dengue NS1 Ag Test, ULTRA Dengue NS1 Ag Test

License Holder

SD Biosensor Healthcare Pvt. Ltd

Device Class

Class C

Approving Authority

Sub Zonal Baddi

Product Information

STANDARD Q COVID-19 IgM/IgG Duo Test is a rapid chromatographic immunoassay for the qualitative detection of specific antibodies to COVID-19 present in human serum, plasma or whole blood

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Dengue virus Antigen Test Kits

Brand: STANDARD Q Dengue NS1 Ag Test, ULTRA Dengue NS1 Ag Test

SD Biosensor Healthcare Pvt. Ltd

Standard Q COVID-19 IgM/IgG DUO - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

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