Reagent Kit for Qualitative and Quantitative Detection of High-Risk Human Papillomavirus (HPV) DNA Types 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68 Using Real-Time PCR

This reagent kit is intended for the qualitative and quantitative detection of high-risk human papillomavirus (HPV) DNA types 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68 using real-time polymerase chain reaction (PCR). The product is labeled as "AmpliPrime® HPV HR 14" and complies with TU 21.20.23-037-09286667-2019.

Kit Components:

HPV Screening PCR Mix – 1.10 ml × 1 tube
Buffer B – 0.60 ml × 1 tube
HPV Screening Control K1 – 0.12 ml × 1 tube
HPV Screening Control K2 – 0.12 ml × 1 tube
Internal Control (ICO) – 1.10 ml × 1 tube
Negative Control (K-) – 0.26 ml × 1 tube
Software "AmpliPrime® HPV HR 14", version 1.0 on USB flash drive – 1 pc
Instructions for use in electronic format on USB flash drive and on the manufacturer's official website: http://www.nextbio.ru/reagents/
Quick Start Guide – in printed format
Package insert – in printed format
Certificate of analysis available electronically at: http://www.nextbio.ru/passport/
Operator’s manual in electronic format on USB flash drive and on the official website: http://www.nextbio.ru/reagents/

If your organization wants to sell medical equipment, medical products or medical consumables in Russia, for example, Reagent Kit for Qualitative and Quantitative Detection of High-Risk Human Papillomavirus (HPV) DNA Types 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68 Using Real-Time PCR, then our information portal MEDCOMMERCE can help you with this. To do this, simply fill out the feedback form by clicking on the link FEEDBACK FORM.

The products posted on our website are approved for use in Russia by the state regulator Roszdravnadzor (Federal Service for Surveillance in Healthcare). The information is for informational purposes only.

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