SNQ Quality Mark

SNQ is built on evidence-based standards, setting trusted quality and safety benchmarks for healthcare, biomedical, health, and animal care services and products.

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About the National Quality Mark

  • Vision & Mission
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Certification Methods

  • Medical Service
  • Biomedical Product
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International Certification

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Organized by|Research Center for Biotechnology and Medicine PolicyOperated by|Kuanglu International Quality Standards Co., Ltd.© 2026 Kuanglu International Quality Standards Co., Ltd. All rights reserved.Privacy Policy
SNQ Quality Mark
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Product Description

  • Built-in Quality Control: Utilizes an internal control targeting the human β-globin to differentiate true negative results from invalid ones caused by PCR inhibitors or insufficient cellular mass

  • Contamination Control: The master mix incorporates dUTP and the AmpErase enzyme, which enzymatically degrades contaminating amplicons from previous PCR runs during the initial heating step to prevent carry-over contamination.

  • Fully automated, qualitative in vitro diagnostic assay utilizing real-time PCR and nucleic acid hybridization.

  • End-to-End Automation: Seamlessly operates on the cobas® 5800, 6800, and 8800 systems.

  • Genotyping & Risk Stratification: Detects 14 high-risk HPV types in a single run. It uniquely provides individual genotyping for HPV 16 and HPV 18 while concurrently reporting the pooled result of 12 other HR-HPV types (31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66,and 68).

  • Specimen Versatility: Broad specimen compatibility, including support for healthcare worker-instructed vaginal self-collection to maximize screening accessibility.

  • Clinical Applications Uses : First-Line Primary Screening: Serves as a standalone primary test to identify women at high risk for cervical cancer or high-grade lesions, driving a proactive prevention strategy. ASC-US Triage: Screens patients with ASC-US in cytology to determine the necessity of colposcopy referral. Co-Testing: Used adjunctively alongside routine cytology to assess the presence or absence of HR-HPV genotypes.


Manufacturer

Roche Molecular Systems, Inc.

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Reagents & Consumables

cobas HPV

The core positioning of this product is as a "first-line primary screening test" to identify women at increased risk for the development of cervical cancer or high-grade disease.
Organization
Roche DiagnosticsLtd.Taiwan
Certification Year
2025
cobas HPV