Rapid Antigen Self Testing Kit for COVID-19 - India CDSCO Medical Device Registration
Rapid Antigen Self Testing Kit for COVID-19 is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000150_dda12582ddbecd9fbac11c194f894f83_2d78b929a9b9b7fb7ee9c5c4aec5eaa7. The license holder is NeoDx Biotech Labs Pvt Ltd, and it is classified as Device Class Class C. The approving authority is Sub Zonal Bangalore.
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License Holder
NeoDx Biotech Labs Pvt LtdDevice Class
Approving Authority
Sub Zonal Bangalore
Product Information
NeoCheck Junior Rapid Antigen Self Testing Kit is a test for detecting nucleocapsid antigen from SARS-CoV-2 in human anterior nasal specimen.
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