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NeuMoDx Cartridge - India CDSCO Medical Device Registration

NeuMoDx Cartridge is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000261_70159d5108ab5e2d2298a0f0ce7b4fa8_2f9667af50bec1f71032370550b10067. 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 Cartridge
UID: IMP/IVD/2022/000261_70159d5108ab5e2d2298a0f0ce7b4fa8_2f9667af50bec1f71032370550b10067

Brand Name

NeuMoDx™ LDT Primer/Probe Strip

License Holder

QIAGEN India Pvt. Ltd

Device Class

Class A

Approving Authority

CDSCO

Product Information

The NeuMoDx™ Cartridge is a proprietary consumable used for the efficacious extraction, purification, amplification, and detection of nucleic acids on the NeuMoDx™ 288 and NeuMoDx™ 96 Molecular Systems (NeuMoDx™ System(NeuMoDx™ LDT Primer/Probe Strip)). The NeuMoDx Cartridge is universally used for all tests processed on NeuMoDx Systems

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