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.
Brand Name
careHPV Test Luminometer
License Holder
QIAGEN India Pvt. LtdDevice Class
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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