THE PERFECT PARTNER TO TRANSFORM
YOUR HPV TESTING NEEDS TO DELIVER
CLINICAL AND OPERATIONAL EFFICIENCIES
THE PERFECT PARTNER TO TRANSFORM
YOUR HPV TESTING NEEDS TO DELIVER
CLINICAL AND OPERATIONAL EFFICIENCIES
For In Vitro Diagnostics Use Only.
Alinity mp is an automated, continuous access, pre-analytical system designed to automate the processing of liquid-based cytology samples to assist with the reduction of manual pre-analytical sample preparation tasks.
Providing continuous access for loading sample vials and unloading output tubes
Reducing hands-on time associated with pre-analytical sample processing
Driving standardization through intuitive, user-driven design with simplified touch points and interactions
Standardizing sample processing with integrated sample integrity technologies
After aspiration of the input samples, the mucoid detector evaluates the end of the pipette tip to determine if any sample material extends beyond the end of the pipette tip.
If sample material is detected extending beyond the pipette tip, the sample is returned to the input vial and aspiration is attempted again with a new pipette tip.
On-board labelling of output tubes:
Advanced pipetting to ensure accurate aspiration and dispensing of samples:
Seven cameras located in the Alinity mp continuously monitor the system during operation.
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Alinity mp automates pre-analytical processing steps for liquid based
cytology vials to prepare samples for the Alinity m HR HPV and Alinity m STI assays.
Alinity m is a fully integrated and automated molecular diagnostics analyzer that uses ReadiFlex technology to deliver the next level of flexibility and efficiency to your lab.
Discover a broad menu and robust assay design to deliver operational efficiency and reliable results.
Learn more about the Alinity m High Risk (HR) HPV assay and view ordering information.
Learn about the ReCalibrate series: Where leading experts share ideas and insights.
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Please be aware that the website you have requested is intended for the residents of a particular country or countries, as noted on that site. As a result, the site may contain information on pharmaceuticals, medical devices and other products or uses of those products that are not approved in other countries or regions.