CDSCO UID MFG/IVD/2023/000064_7eb6ca523f55944d511fd8b9975d66b1_7447a1466eafbfb9cf01b60cbe4b89c1

Nucleic Acid Amplification Analyzer

Mylab Discovery Solutions Pvt. Ltd.·Device Class Class A·India CDSCO·Brand: PCR
Registration details
UID
MFG/IVD/2023/000064_7eb6ca523f55944d511fd8b9975d66b1_7447a1466eafbfb9cf01b60cbe4b89c1
Device class
Class A
Brand name
PCR
Approving authority
Pune Division
Product information
It is used for qualitative and quantitative detection of analytes in nucleic acid samples (PCR) from human body, including pathogens and human gene items. Fluorescent Quantitative PCR Detection System features high-quality optical and thermal modules to provide optimal performance. Fluorescent Quantitative PCR Detection System is intended to support the Real- Time polymerase chain reaction (PCR) application needs of life science researchers
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About this record

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_7447a1466eafbfb9cf01b60cbe4b89c1. 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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