KARWA COVID-19 RT-LAMP DIAGNOSTIC KIT - India CDSCO Medical Device Registration
KARWA COVID-19 RT-LAMP DIAGNOSTIC KIT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000004_754d6bb7b58d01c017428c83bf519f11_a4e159da251274b73e7598576a4a74ac. The license holder is KARWA ENTERPRISES PRIVATE LIMITED, and it is classified as Device Class Class C. The approving authority is CDSCO -North Zone, Ghaziabad.
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License Holder
KARWA ENTERPRISES PRIVATE LIMITEDDevice Class
Approving Authority
CDSCO -North Zone, Ghaziabad
Product Information
Intended for qualitative detection of nucleic acid from SARS-CoV-2 RNA in throat and or nasal swab samples who are suspected of COVID-19
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