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NeuMoDx™ HCV Calibrators - India CDSCO Medical Device Registration

NeuMoDx™ HCV Calibrators is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000261_9d1a29c2e12d1c9ec192e0f83b787f33_5e5534eca5a828c3683b3de8a4f10167. This device is marketed under the brand name NeuMoDx™ HCV Calibrators. The license holder is QIAGEN India Pvt. Ltd, and it is classified as Device Class Class C. The approving authority is CDSCO.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class C
NeuMoDx™ HCV Calibrators
UID: IMP/IVD/2022/000261_9d1a29c2e12d1c9ec192e0f83b787f33_5e5534eca5a828c3683b3de8a4f10167

Brand Name

NeuMoDx™ HCV Calibrators

License Holder

QIAGEN India Pvt. Ltd

Device Class

Class C

Approving Authority

CDSCO

Product Information

The NeuMoDx™ HCV Calibrators are a component of the NeuMoDx™ HCV Quant Assay, an in vitro diagnostic nucleic acid amplification test intended for the detection and quantitation of hepatitis C virus (NeuMoDx™ HCV Calibrators) RNA in human plasma and serum

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