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Nucleic Acid Amplification Analyzer - India CDSCO Medical Device Registration

Nucleic Acid Amplification Analyzer is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000064_7eb6ca523f55944d511fd8b9975d66b1_e7a3abdd7e9428739115dc4d22f88f89. This device is marketed under the brand name PCR. The license holder is Mylab Discovery Solutions Pvt. Ltd., and it is classified as Device Class Class A. The approving authority is Pune Division.

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CDSCO Registered
Class Class A
Nucleic Acid Amplification Analyzer
UID: MFG/IVD/2023/000064_7eb6ca523f55944d511fd8b9975d66b1_e7a3abdd7e9428739115dc4d22f88f89

Brand Name

PCR

Device Class

Class A

Approving Authority

Pune Division

Product Information

This instrument is designed for extraction, purification, amplification of target DNA/RNA and qualitative and quantitative detection of analytes. The instrument is intended to be used to automate lab operations from sample handling to results. It has a flexibility to test multiple parameters with multiple samples at the same time. The Automated nucleic acid extraction and qPCR analysis system is a sample-to-result system that eliminates huge infrastructure cost of setting up a molecular lab

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DJ Fang

DJ Fang

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