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NeuMoDx™ LDT Master Mix, RNA - India CDSCO Medical Device Registration

NeuMoDx™ LDT Master Mix, RNA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000261_6db6deb7787b4ba6fc1801034b5a2148_b396fc068b104c450ac98acf8c6fffa4. This device is marketed under the brand name NeuMoDx™ LDT Primer/Probe Strip. The license holder is QIAGEN India Pvt. Ltd, and it is classified as Device Class Class A. 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 A
NeuMoDx™ LDT Master Mix, RNA
UID: IMP/IVD/2022/000261_6db6deb7787b4ba6fc1801034b5a2148_b396fc068b104c450ac98acf8c6fffa4

Brand Name

NeuMoDx™ LDT Primer/Probe Strip

License Holder

QIAGEN India Pvt. Ltd

Device Class

Class A

Approving Authority

CDSCO

Product Information

The NeuMoDx LDT Master Mix, RNA is a 16-well strip containing a proprietary, room temperature stable, real-time RT-PCR master mix that, when used in conjunction with assay specific primers and probe(NeuMoDx™ LDT Primer/Probe Strip), enables a laboratory to rapidly develop and implement laboratory developed tests (NeuMoDx™ LDT Primer/Probe Strip) on the NeuMoDx 288 Molecular System and NeuMoDx 96 Molecular System (NeuMoDx System(NeuMoDx™ LDT Primer/Probe Strip)). Other than the LDT-specific primers and probe(NeuMoDx™ LDT Primer/Probe Strip), the NeuMoDx LDT Master Mix, RNA incorporates all the reagents required for real-time RT-PCR. Once validated by the user’s laboratory as part of the LDT, this reagent can be used as a key component for rapid automation of the LDT

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