Nucleic Acid Amplification Analyzer(Compact Q ) - India CDSCO Medical Device Registration

Nucleic Acid Amplification Analyzer(Compact Q ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000062_7ffaa2a37c75b74bc40124a5f4e8d5a4_5c5557407ab9673b11e44c2cdb65fc50. This device is marketed under the brand name PCR. The license holder is Mylab Discovery Solutions Pvt. Ltd. Lonavla, 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(Compact Q )

UID: MFG/IVD/2021/000062_7ffaa2a37c75b74bc40124a5f4e8d5a4_5c5557407ab9673b11e44c2cdb65fc50

Brand Name

PCR

License Holder

Mylab Discovery Solutions Pvt. Ltd. Lonavla

Device Class

Class A

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

Class A

Fluorescent Immunoassay Analyser

Brand: PCR

Mylab Discovery Solutions Pvt. Ltd. Lonavla

Class A

Brand: hCG

Class B