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careHPV Test Luminometer - India CDSCO Medical Device Registration

careHPV Test Luminometer is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000376_af4ff4bfb26b0b0588dbefe899c85d14_ee33394d60f935f40b90631bdc36ce27. This device is marketed under the brand name careHPV Test Luminometer . 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
careHPV Test Luminometer
UID: IMP/IVD/2022/000376_af4ff4bfb26b0b0588dbefe899c85d14_ee33394d60f935f40b90631bdc36ce27

Brand Name

careHPV Test Luminometer

License Holder

QIAGEN India Pvt. Ltd

Device Class

Class A

Approving Authority

CDSCO

Product Information

The careHPV Test System instruments are intended to be used only in combination with QIAGEN kits indicated for use with the careHPV Test System instruments for the applications described in the kit handbooks. The careHPV Test System instruments are intended for use by professional users, such as technicians and physicians trained in molecular biological techniques and the operation of the careHPV Test System

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DJ Fang

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