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DIAGNOSTICS TEST REAGENT/ KITS FOR DENGUE NS1. - India CDSCO Medical Device Registration

DIAGNOSTICS TEST REAGENT/ KITS FOR DENGUE NS1. is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000009_f8574ff71e52346e1c2bb4435897c9f4_1d59f725579c315f1336c05577888f0d. This device is marketed under the brand name Covid-19 RT PCR. The license holder is Vimek Bioconcept Pvt Ltd, 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
DIAGNOSTICS TEST REAGENT/ KITS FOR DENGUE NS1.
UID: MFG/IVD/2022/000009_f8574ff71e52346e1c2bb4435897c9f4_1d59f725579c315f1336c05577888f0d

Brand Name

Covid-19 RT PCR

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

Rapid Dengue NS1 antigen test is an Later Flow assay for the qualitative detection of non-structural protein 1 ( Covid-19 RT PCR) in human serum/plasma/ whole blood

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