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CDSCO UID IMP/IVD/2023/000088_8c4e6e23734afe3cf0bbe804263e07db_e77b7f9db0caaa3c5a0876380f30e54b

QIAscreen HPV PCR Test

QIAGEN India Pvt. Ltd·Device Class Class C·India CDSCO·Brand: QIAscreen HPV PCR Test
Registration details
UID
IMP/IVD/2023/000088_8c4e6e23734afe3cf0bbe804263e07db_e77b7f9db0caaa3c5a0876380f30e54b
Device class
Class C
Brand name
QIAscreen HPV PCR Test
License holder
QIAGEN India Pvt. Ltd
Approving authority
CDSCO
Product information
The QIAscreen HPV PCR Test is an in vitro real-time PCR-based assay for the qualitative detection of human papillomavirus (QIAscreen HPV PCR Test) DNA of the following 15 (QIAscreen HPV PCR Test) high-risk HPV genotypes, i.e 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 67, and 68. The assay is intended to be used for the screening of women for the risk of cervical (QIAscreen HPV PCR Test)cancer.
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About this record

QIAscreen HPV PCR Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000088_8c4e6e23734afe3cf0bbe804263e07db_e77b7f9db0caaa3c5a0876380f30e54b. This device is marketed under the brand name QIAscreen HPV PCR Test. The license holder is QIAGEN India Pvt. Ltd, and it is classified as Device Class Class C. The approving authority is CDSCO.

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