BIOLINE HAV IgG/IgM - India CDSCO Medical Device Registration

BIOLINE HAV IgG/IgM is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000156_10abf79ed0e0dce593be3525f15436ea_af3ff5b8ec6e1c781055880c41630d3b. This device is marketed under the brand name SD BIOLINE Dengue IgG/IgM WB. The license holder is Abbott Diagnostics Medical Private Limited, and it is classified as Device Class Class B. The approving authority is CDSCO.

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CDSCO Registered

Class Class B

BIOLINE HAV IgG/IgM

UID: IMP/MD/2018/000156_10abf79ed0e0dce593be3525f15436ea_af3ff5b8ec6e1c781055880c41630d3b

Brand Name

SD BIOLINE Dengue IgG/IgM WB

License Holder

Abbott Diagnostics Medical Private Limited

Device Class

Class B

Approving Authority

CDSCO

Product Information

BIOLINE HAV IgG/IgM Rapid Test is a solid phase immunochromatographic assay for the rapid, qualitative and differential detection of IgG and IgM antibodies to Hepatitis A virus in human serum or plasma

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