CDSCO UID MFG/IVD/2020/000057_7b2548ce54951d0031cf42487d2ca6f7_a1a6a9a9f198a39daff336305598ad8d

Dengue NS1 Rapid Antigen Test

Cadila Healthcare Limited·Device Class Class C·India CDSCO·Brand: ZyDx Anti-SARS CoV-2-IgG Antibody Detection ELISA
Registration details
UID
MFG/IVD/2020/000057_7b2548ce54951d0031cf42487d2ca6f7_a1a6a9a9f198a39daff336305598ad8d
Device class
Class C
Brand name
ZyDx Anti-SARS CoV-2-IgG Antibody Detection ELISA
Approving authority
Central Drug Standards Control Organization, Ahmedabad
Product information
Dengue NS1 Rapid Antigen Test is a solid phase Immuno-chromatographic assay intended for qualitative detection of dengue infection by Dengue NS1 Antigen in Human Blood, Serum or Plasma samples.
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About this record

Dengue NS1 Rapid Antigen Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000057_7b2548ce54951d0031cf42487d2ca6f7_a1a6a9a9f198a39daff336305598ad8d. This device is marketed under the brand name ZyDx Anti-SARS CoV-2-IgG Antibody Detection ELISA. The license holder is Cadila Healthcare Limited, and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, Ahmedabad.

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