HCG+Beta(HCG+Beta Fast Test Kit ) - India CDSCO Medical Device Registration
HCG+Beta(HCG+Beta Fast Test Kit ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000016_f8ab15b36d4c34ee2d232780e03046f0_d762428e0e353930d7060718bc3d9920. This device is marketed under the brand name Immunofluorescence Assay. The license holder is Akshat Bio Medicals Pvt Ltd, and it is classified as Device Class Class B. The approving authority is CDSCO.
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Brand Name
Immunofluorescence Assay
License Holder
Akshat Bio Medicals Pvt LtdDevice Class
Approving Authority
CDSCO
Product Information
HCG+Beta fast test kit (Immunofluorescence Assay) is intended for in vitro quantitative determination of human chorionic gonadotropin (Immunofluorescence Assay) in serum and plasma. This test is used as aid in pregnancy test
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