Skip to main content Skip to navigation

BD FACSDuet™ Sample Preparation System

Overview

The BD FACSDuet™ sample preparation system provides a powerful new level of performance to move the pace of your lab forward. With pre-analytical automation with standardisation, the BD FACSDuet™ drives consistency and workflow efficiency. The BD FACSDuet™ also allows for automated cocktail preparation, greatly enhancing the flexibility and standardization.  Designed to complement and physically integrate with the BD FACSLyric™ flow cytometer, the BD FACSDuet™ provides a complete walkaway sample-to-answer solution. Through its automation protocol, the BD FACSDuet™ enables higher lab productivity and accuracy in results by minimising manual intervention. The complete workflow traceability provided by the BD FACSDuet™ enables the lab to be compliant with ISO-15189 standards.

Request Demo
 
performance1

Features

prev
next

“What is the potential impact of the BD FACSDuet? It removes our manual processes, increases our efficiency and throughput, and gives us control in standardization of processes. It’s a controlled environment”

“What is the potential impact of the BD FACSDuet? It removes our manual processes, increases our efficiency and throughput, and gives us control in standardization of processes. It’s a controlled environment”

Mr. D. Bloxham
Principle Biomedical Scientist
ODS Cambridge University Hospital NHS Trust – Cambridge - UK

“I require all the monoclonal antibodies used, the ancillary reagents, tubes, the QC materials to be linked to an exact patient…this is an essential laboratory process and it is also mandatory in order to maintain ISO 15189 accreditation"

“I require all the monoclonal antibodies used, the ancillary reagents, tubes, the QC materials to be linked to an exact patient…this is an essential laboratory process and it is also mandatory in order to maintain ISO 15189 accreditation"

Mr. C. Scott
Lead Biomedical Scientist, Immunology Dep.
Barts Health NHS Trust, UK
prev
next

BD FACSDuet™ is CE marked in compliance with the European In Vitro Diagnostic Medical Device Directive 98/79/EC.