Reagent Kit for Quantitative Detection of High-Risk Human Papillomavirus (HPV) DNA Genotypes 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68 by PCR for In Vitro Diagnostics “AmpliSens® HPV HR Screen-Titer-14-FL” (TU 9398-231-01897593-2015)

Reagent Kit for Quantitative Detection of High-Risk Human Papillomavirus (HPV) DNA Genotypes 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68 by PCR for In Vitro Diagnostics “AmpliSens® HPV HR Screen-Titer-14-FL” (TU 9398-231-01897593-2015)

This reagent kit is intended for the quantitative detection of DNA from high-risk human papillomavirus (HPV) genotypes 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68 in biological samples using polymerase chain reaction (PCR) for in vitro diagnostic applications.

Available Configuration:

• Form 1: Includes the “PCR Kit” variant FRT-100 FN.

Kit Contents:

• PCR Mix-FL HPV 14 – 1 tube
• PCR Buffer-N – 1 tube
• K1 HPV Screen – 1 tube
• K2 HPV Screen – 1 tube
• K– (Negative Control) – 1 tube

If your organization wants to sell medical equipment, medical products or medical consumables in Russia, for example, Reagent Kit for Quantitative Detection of High-Risk Human Papillomavirus (HPV) DNA Genotypes 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, 68 by PCR for In Vitro Diagnostics “AmpliSens® HPV HR Screen-Titer-14-FL” (TU 9398-231-01897593-2015), 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.