Dengue Ag ELISA Kit - India CDSCO Medical Device Registration

Dengue Ag ELISA Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000034_08236454d6872dab58e6ae35ed46df2b_3c5955a8352c5bc61d49901b328b5773. This device is marketed under the brand name Aridia. The license holder is Athenese-Dx Private Limited, and it is classified as Device Class Class C. The approving authority is Central Drug Standard Control Organisation, South Zone.

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CDSCO Registered

Class Class C

Dengue Ag ELISA Kit

UID: MFG/IVD/2020/000034_08236454d6872dab58e6ae35ed46df2b_3c5955a8352c5bc61d49901b328b5773

Brand Name

Aridia

License Holder

Athenese-Dx Private Limited

Device Class

Class C

Approving Authority

Central Drug Standard Control Organisation, South Zone

Product Information

The Dengue Ag (Aridia) ELISA is a solid-phase enzyme-linked immunosorbent assay for the qualitative detection of dengue NS1 antigen (Aridia) in human serum or plasma. It is intended for professional use only as an aid in the diagnosis of an acute infection with dengue viruses

Class C

Brand: TRUSTline

Class D