Rotor-Gene Q MDx 6plex - India CDSCO Medical Device Registration
Rotor-Gene Q MDx 6plex is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000376_b79f11230d789180c7acee5bf2d4a229_3fa077e507eb29fb81b71402b5450558. 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.
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Brand Name
careHPV Test Luminometer
License Holder
QIAGEN India Pvt. LtdDevice Class
Approving Authority
CDSCO
Product Information
The Rotor-Gene Q MDx instrument is designed to perform real-time thermal cycling, detection, and/or quantification using the polymerase chain reaction (careHPV Test Luminometer ) in clinical applications. The Rotor-Gene Q MDx is intended to be used only in combination with QIAGEN kits indicated for use with Rotor-Gene Q instruments for applications described in the respective QIAGEN kit handbooks. If the Rotor-Gene Q MDx instrument is used with other than QIAGEN Kits, it is the userโs responsibility to validate the performance of such product combination for any particular application. The Rotor-Gene Q MDx instrument is intended for in vitro diagnostic use. The Rotor-Gene Q MDx instrument is intended for use by professional users, such as technicians and physicians trained in molecular biological techniques and the operation of the Rotor-Gene Q MDx instrument.,careHPV Test Shaker (careHPV Test Luminometer )-The careHPV Test Shaker is a heating and shaking instrument that contains nonadjustable heating elements in the lid and in the microplate holder in the bottom. The careHPV Test Shaker heats and shakes a 96-well microplate. The careHPV Test Shaker features the following: โข Fast heating of the top and bottom of the microplate โข Regulated orbital shaking
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