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HEV RT-PCR Kit 1.5 - India CDSCO Medical Device Registration

HEV RT-PCR Kit 1.5 is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/001064_1f6ec98336cc3a2f27346bbd33bb7682_e3ab5c0a705ae1567d3403d5313a3f22. This device is marketed under the brand name AltoStar®. The license holder is Altona Diagnostics India Pvt. Ltd., and it is classified as Device Class Class C. The approving authority is CDSCO.

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CDSCO Registered
Class Class C
HEV RT-PCR Kit 1.5
UID: IMP/IVD/2020/001064_1f6ec98336cc3a2f27346bbd33bb7682_e3ab5c0a705ae1567d3403d5313a3f22

Brand Name

AltoStar®

Device Class

Class C

Approving Authority

CDSCO

Product Information

The AltoStar® HEV RT-PCR Kit 1.5 is an in vitro diagnostic test, based on real time PCR technology, for the detection and quantification of hepatitis E virus (AltoStar®) specific RNA in human plasma. The AltoStar® HEV RT-PCR Kit 1.5 is configured for use with the CFX96™ Deep Well Dx System (AltoStar®) in combination with the AltoStar® Automation System AM16, the AltoStar® Purification Kit 1.5 and the AltoStar® Internal Control 1.5. The results generated with the AltoStar® HEV RT-PCR Kit 1.5 have to be interpreted in conjunction with other clinical and laboratory findings. The AltoStar® HEV RT-PCR Kit 1.5 is intended for use by professional users trained in molecular biological techniques

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