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NeuMoDx Viral Lysis Buffer - India CDSCO Medical Device Registration

NeuMoDx Viral Lysis Buffer is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000261_73b8ad3381ea2e2bbc0584e5d6ab9bd2_cab1b1ce0d07d02e740b5bf32c04d022. 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.

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CDSCO Registered
Class Class A
NeuMoDx Viral Lysis Buffer
UID: IMP/IVD/2022/000261_73b8ad3381ea2e2bbc0584e5d6ab9bd2_cab1b1ce0d07d02e740b5bf32c04d022

Brand Name

NeuMoDx™ LDT Primer/Probe Strip

License Holder

QIAGEN India Pvt. Ltd

Device Class

Class A

Approving Authority

CDSCO

Product Information

NeuMoDx™ Viral Lysis Buffer is intended for the pretreatment of respiratory specimens in UTM-RT® or equivalent prior to processing on the NeuMoDx™ 288 Molecular System or NeuMoDx™ 96 Molecular System (NeuMoDx™ System(NeuMoDx™ LDT Primer/Probe Strip))

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