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SurePath™ Liquid-Based Cytology System
The SurePath™ LBC system uses a proprietary sample collection method and patented centrifugal sedimentation technology — the third-generation cytology testing method. It delivers automated, standardised, high-throughput slide preparation with industry-leading specimen adequacy rates and the highest FDA-certified cancer precursor detection rate compared to conventional Pap smears.
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Affirm™ VPIII Vaginal Infections Microbial Detection System
The Affirm™ VPIII is the industry's first fully automated system using DNA probe technology to simultaneously detect the three most common vaginal pathogens — Bacterial Vaginosis (BV), Vulvovaginal Candidiasis (VVC) and Trichomonas Vaginalis (TV) — from a single sample. It has become the standard method for vaginal infection testing recommended by the US Centers for Disease Control and Prevention (CDC).
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Viper LT™ System & Onclarity™ HPV Assay
The Viper LT™ is a benchtop molecular platform that automates DNA extraction, RT-PCR amplification, detection and result reporting — minimising manual intervention. Paired with the Onclarity™ HPV Assay, it delivers genotyping results for 14 high-risk HPV types, with individual identification of 6 types, from the same SurePath™ vial used for liquid-based cytology — one sample, two tests.
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DNA Ploidy Analysis System
The DNA Ploidy Analysis System combines with SurePath™ liquid-based cytology to create a dual-modality cervical cancer screening solution — one preparation, two tests. Automated quantitative DNA ploidy analysis detects chromosomal abnormalities at the molecular level, identifying occult lesions that conventional cytology may miss, and raising CIN2+ detection sensitivity to 96.9%.
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