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CDSCO UID MFG/IVD/2020/000024_bd91d4bb28a1e3b34281f85ddc4f3e1c_bf06fd2ff991a3e3927f8047f5f5cd3a

Detection of Novel Coronavirus 2019-nCoV/SARS-CoV-2 from clinical samples(TRUPCR® SARS-CoV-2 RT qPCR Kit )

KILPEST INDIA LIMITED·Device Class Class C·India CDSCO·Brand: TRURAPID® Dengue NS-1 Ag Test
Registration details
UID
MFG/IVD/2020/000024_bd91d4bb28a1e3b34281f85ddc4f3e1c_bf06fd2ff991a3e3927f8047f5f5cd3a
Device class
Class C
Brand name
TRURAPID® Dengue NS-1 Ag Test
License holder
KILPEST INDIA LIMITED
Approving authority
Central Drug Standards Control Organization, West Zone
Product information
TRUPCR® SARS-CoV-2 RT qPCR kit (TRURAPID® Dengue NS-1 Ag Test) is an in-vitro nucleic acid amplification test for the qualitative detection of severe acute respiratory syndrome coronavirus 2 (TRURAPID® Dengue NS-1 Ag Test) specific RNA from respiratory specimens (TRURAPID® Dengue NS-1 Ag Test) using Real time PCR. The human RNaseP gene serves as an internal positive control for human nucleic acid, also included in this kit. The result from TRUPCR® SARS-CoV-2 RT qPCR kit (TRURAPID® Dengue NS-1 Ag Test) should be interpreted in conjunction with other clinical and laboratory findings
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About this record

Detection of Novel Coronavirus 2019-nCoV/SARS-CoV-2 from clinical samples(TRUPCR® SARS-CoV-2 RT qPCR Kit ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000024_bd91d4bb28a1e3b34281f85ddc4f3e1c_bf06fd2ff991a3e3927f8047f5f5cd3a. This device is marketed under the brand name TRURAPID® Dengue NS-1 Ag Test. The license holder is KILPEST INDIA LIMITED, and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, West Zone.

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