HCG+ Beta Fast Test Kit - India CDSCO Medical Device Registration

HCG+ Beta Fast Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000410_fe793d28bc85867c022be4652e478f06_dc66ef4ae26a72a9435f61663a6fffa6. This device is marketed under the brand name Imumunofluorescence Assay. The license holder is Vector Biotek Pvt Ltd, and it is classified as Device Class Class B. The approving authority is CDSCO.

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CDSCO Registered

Class Class B

HCG+ Beta Fast Test Kit

UID: IMP/IVD/2019/000410_fe793d28bc85867c022be4652e478f06_dc66ef4ae26a72a9435f61663a6fffa6

Brand Name

Imumunofluorescence Assay

License Holder

Vector Biotek Pvt Ltd

Device Class

Class B

Approving Authority

CDSCO

Product Information

HCG+beta Fast Test Kit (Imumunofluorescence Assay) is intended for in vitro quantitative determination of human chorionic gonadotropin (Imumunofluorescence Assay) in serum or plasma. This test is used as an aid in pregnancy test.,mAlb Fast Test Kit (Imumunofluorescence Assay)(Imumunofluorescence Assay)-mAlb Fast Test Kit (Imumunofluorescence Assay) is intended for in vitro quantitative determination of microalbuminuria (Imumunofluorescence Assay) in urine. An elevated mAlb concentration below the proteinuric level has long been recognized as a marker of kidney disease and increased cardiovascular risk in diabetic nephropathy

Class B

NT-proBNP Fast Test Kit

Brand: Imumunofluorescence Assay

Vector Biotek Pvt Ltd

Class C

Brand: MAGLUMI

Class B