Covid-19 RT-PCR reagents and kits - India CDSCO Medical Device Registration

Covid-19 RT-PCR reagents and kits is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000041_d33eaad4ed534e0a65f21f0e75b40c65_d02256e34a9f730d18858bb72265c738. This device is marketed under the brand name Pv/Pf. The license holder is BIOSCI HEALTH CARE, and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, West Zone.

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CDSCO Registered

Class Class C

Covid-19 RT-PCR reagents and kits

UID: MFG/IVD/2021/000041_d33eaad4ed534e0a65f21f0e75b40c65_d02256e34a9f730d18858bb72265c738

Brand Name

Pv/Pf

License Holder

BIOSCI HEALTH CARE

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

The BioSci True Detect Covid-19 RT-PCR Test is a real-time reverse transcription-PCR assay for the qualitative detection of SARS-CoV-2 nucleic acids in nasopharyngeal, oropharyngeal, nasal, and mid- turbinate nasal swab, and sputum