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NeuMoDx Release Reagent - India CDSCO Medical Device Registration

NeuMoDx Release Reagent is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000261_46223d4eb2e81e2d5a8a5881f77ef616_918e11f9f780cb265570ca32b7da4333. 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 Release Reagent
UID: IMP/IVD/2022/000261_46223d4eb2e81e2d5a8a5881f77ef616_918e11f9f780cb265570ca32b7da4333

Brand Name

NeuMoDx™ LDT Primer/Probe Strip

License Holder

QIAGEN India Pvt. Ltd

Device Class

Class A

Approving Authority

CDSCO

Product Information

The NeuMoDx™ Release Reagent is a proprietary reagent used for the efficacious extraction of nucleic acids on the NeuMoDx™ 288 Molecular System and NeuMoDx™ 96 Molecular System (NeuMoDx™ System(NeuMoDx™ LDT Primer/Probe Strip)) in conjunction with other NeuMoDx™ reagents, such as the NeuMoDx™ Extraction Plate, NeuMoDx™ Lysis Buffers, and NeuMoDx™ Wash Reagent

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