PD49 Poly Diagnostics HSV-1/2, CMV, HPV-16/18, RNase P Real-Time PCR kit

Ready-to-use multiplex real-time PCR kit for simultaneous detection and differentiation of Human Herpes Simplex Virus 1 and 2 in clinical specimens. Enables rapid molecular diagnosis of HSV infections with CE marking compliance for in vitro diagnostic use.

RTA HSV-1&2 Multiplex Real-Time PCR Kit is a multiplex in vitro nucleic acid amplification test designed for simultaneous detection of Herpes Simplex Virus Type 1 and Type 2 (HSV-1 and HSV-2) DNA from human serum samples. It targets different sequences in the Glycoprotein G region of HSV-1 and HSV-2 genomes and uses WHO CE-marked reference materials for standardization. The kit is used to assist in directing treatment for transplant patients with potential Herpes Simplex 1 and 2 infection alongside other relevant clinical and laboratory findings.

CE-IVD qPCR detection kit for rapid identification of Herpes Simplex Virus Type 1 and Type 2 in blood and tissue samples. Enables confident molecular diagnosis of HSV infections through quantitative PCR technology for clinical and laboratory settings.

Real-time PCR detection kit for Herpes Simplex Virus types 1 and 2. Enables rapid diagnosis and differentiation of HSV infections.

Multiplex real-time PCR kit for simultaneous detection and typing of human papillomavirus (HPV) 16 and 18 strains. Used in clinical diagnostics for cervical cancer screening and HPV genotyping. Enables rapid, multiplexed analysis from patient samples with high sensitivity and specificity.

CE-IVD marked qPCR detection kit for identification of Human Papillomavirus types 16 and 18 in clinical samples. Enables rapid molecular diagnosis of high-risk HPV strains associated with cervical and anogenital cancers. Suitable for use in clinical laboratories and diagnostic facilities performing HPV screening and risk stratification.

A fully enclosed diagnostic kit with preloaded reagents for 6-plex detection of HPV types (HPV16, HPV18, and others) using cervical exfoliated cells and genital secretion samples. The kit employs magnetic beads extraction, purification, and qPCR method with results available within 2 hours and internal control monitoring throughout the process. It requires no freezer storage or transportation.

Molecular diagnostic test for human papillomavirus detection using polymerase chain reaction technology. Enables nucleic acid-based identification of HPV pathogens for clinical screening applications.

PCR-based human papillomavirus detection assay capable of identifying 23 HPV genotypes including 18 high-risk and 5 low-risk variants for cervical cancer screening and auxiliary diagnosis.

This diagnostic kit uses real-time multiple fluorescent PCR technology combined with an Automated Fully Enclosed qPCR Instrument. It is used for in vitro qualitative detection of high-risk HPV16, HPV18, and 16 other high-risk types (HPV26, HPV31, HPV33, HPV35, HPV39, HPV45, HPV51, HPV52, HPV53, HPV56, HPV58, HPV68, HPV59, HPV66, HPV73, and HPV82) in cervical exfoliated cells or reproductive tract secretions. Test results assist in HPV auxiliary diagnosis.

Multiplex real-time PCR kit for simultaneous detection and genotyping of 28 HPV types. Enables comprehensive cervical cancer screening and risk stratification through E6/E7 mRNA analysis. Delivers rapid, multiplexed results for clinical HPV surveillance and patient management.

A real-time PCR reagent kit for the detection and differentiation of human papillomavirus types 16, 18, and 45 DNA with quantitative detection capabilities.