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Dengue IgM /IgG Rapid and Precise Card Test. Detection of Dengue IgM and IgG antibodies in Human serum, plasma or Whole Blood - India CDSCO Medical Device Registration

Dengue IgM /IgG Rapid and Precise Card Test. Detection of Dengue IgM and IgG antibodies in Human serum, plasma or Whole Blood is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000106_8fc256798c5069aa616000e5603217b9_650e6925796afe47df159085ffe1a45f. This device is marketed under the brand name Qualax. The license holder is ADVY CHEMICAL PVT. LTD., and it is classified as Device Class Class B. The approving authority is Kokan Division.

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CDSCO Registered
Class Class B
Dengue IgM /IgG Rapid and Precise Card Test. Detection of Dengue IgM and IgG antibodies in Human serum, plasma or Whole Blood
UID: MFG/IVD/2020/000106_8fc256798c5069aa616000e5603217b9_650e6925796afe47df159085ffe1a45f

Brand Name

Qualax

Device Class

Class B

Approving Authority

Kokan Division

Product Information

EzDx Dengue IgM / IgG Rapid and Precise Card Test is intended for Detection of Dengue IgM and IgG antibodies in Human serum, plasma or Whole Blood. The assay is used as a screening test for Dengue Viral Infection and as an aid in differential diagnosis of primary and secondary infections in conjunction with other criteria

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