The BD MAX™ system offers you an efficient path to improved clinical outcomes by combining and automating extraction and thermocycling into a single platform capable of running both FDA-cleared and Health Canada-cleared and open system assays. Flexibility and standardization allow you to address the breadth of your testing needs.
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BD MAX™ system
Redefine staff productivity with a fully integrated, automated molecular platform
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Accuracy
The system provides highly sensitive and specific results through real-time PCR technology, and consistent results through standardized workflow and protocols.
Improved outcomes
Rapidly expanding menu and open system options help you address emerging testing needs.
Flexibility
- The system is capable of running multiple specimen types and assays in a single run.
- The system is capable of running both FDA-cleared and open system assays.
Efficiency
- The system provides onboard lysis and extraction with pre-filled reagent strips, requiring less than one minute of hands-on time per sample.
- The system features integrated and fully automated extraction and thermocycling steps.
Ease of use
The system is CLIA moderately complex and easy to use.
BD MAX™ System Service Offerings
BD Technical Services is your partner for performance. BD Service teams enable you to better serve your customers and patients. You can count on our deep knowledge and experience to help ensure your BD MAX™ System delivers expected, timely results.
BD MAX™ System Brochure
BD Life Sciences Technical Services
BD Service teams enable you to better serve your customers, patients and research partners. You can count on our deep knowledge and experience to help ensure your instruments deliver expected, timely results.
BD Life Sciences RSS Remote Connectivity
Remote Support Services (RSS) is the BD enterprise-class solution offering remote management and support of BD products deployed at your clinical and research laboratory.
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Notes
The BD MAX system is cleared or approved by the U.S. FDA only when used with BD MAX™ IVD assays, which have been cleared or approved by the FDA. IVD assays, research use only (RUO) assays and user-defined protocols (UDP) cannot be combined in the same rack.
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