QIAstat-Dx US

• Intuitive workflow with minimal hands-on time
• Uses RT-PCR to deliver comprehensive results in about an hour
• Provides Ct values and amplification curves for all detected pathogens directly on the instrument touchscreen
• No precision pipetting required
• QIAsphere-connected for real-time updates and custom epidemiology reports*

QIAstat-Dx simplifies infectious disease diagnostics so you can get faster results for your patients. All you need are a patient sample, a QIAstat-Dx assay cartridge and our intuitive QIAstat-Dx instrument.

The QIAstat-Dx assay cartridges use multiplex real-time (RT) PCR technology – also known as syndromic testing – to quickly survey many different pathogens in a single patient sample. The cartridges come ready with all reagents preloaded and use our trusted assay chemistry to provide comprehensive results in about an hour.

The QIAstat-Dx Analyzer 2.0 is our flexible modular system, perfect for labs of every size. Each instrument is made up of 1 Operational Module PRO, which contains the intuitive touchscreen interface, and between 1 to 4 Analytical Modules, letting you test up to 4 samples at once (see "A flexible modular setup to meet your needs"). 

Save time in the lab and streamline your testing with QIAstat-Dx connectivity, powered by QIAsphere*. With QIAsphere, you can:

• Remotely monitor your instruments in real-time and get test status updates sent to your mobile devices
• Access on-demand epidemiology reports to support your institution-wide surveillance efforts
• Reduce instrument downtime with remote troubleshooting and maintenance

Visit our resource hub to learn how syndromic testing with QIAstat-Dx can help you provide the best care possible for your patients.

*Some features require a QIAstat-Dx Connectivity plan. Flexible plans are available to meet your needs.

The QIAstat-Dx Analyzer 2.0, combined with QIAstat-Dx assay cartridges, use real-time PCR to detect pathogen nucleic acids in human biological samples. The QIAstat-Dx Analyzer 2.0 and cartridges are designed as closed systems that contain all necessary reagents, enabling hands-off sample preparation. Detected real-time amplification signals are interpreted by the integrated software and are reported via an intuitive user interface.

Setting up and running a QIAstat-Dx test requires minimal hands-on time and just a few simple steps (see " Multiplex panel testing doesn't get easier than this").

1. Add the patient sample to the main port of the QIAstat-Dx cartridge using the plastic pipette provided. This step is fast and easy to perform and requires no precision pipetting.
2. Press the Run Test button on the QIAstat-Dx touch screen and scan the sample ID barcode.
3. Scan the barcode of the cartridge you’re using.
4. For our QIAstat-Dx Gastrointestinal Panel 2 test, select the sample type (Para-Pak C&S or FecalSwab).
5. Position the cartridge on the instrument’s sample port. The cartridge will automatically move in and the test will start.
6. After about an hour, view the comprehensive results.

QIAstat-Dx Respiratory Panel Plus: Our FDA-cleared test to analyze 21 viral and bacterial targets for common pathogens causing respiratory symptoms, including SARS-CoV-2. 

This version of our assay replaces the QIAstat-Dx Respiratory SARS-CoV-2 Panel. 

QIAstat-Dx Respiratory Panel Mini: Our FDA-cleared test to analyze 5 viral targets for common pathogens causing respiratory symptoms, including Human Rhinovirus. 

QIAstat-Dx Gastrointestinal Panel 2: Our FDA-cleared test to analyze 16 bacterial, viral and parasitic targets for common pathogens causing gastrointestinal symptoms using preserved stool samples (Para-Pak C&S and FecalSwab)**. 

** STEC and EPEC results are not reported for stool specimens collected in FecalSwab transport media.

***Also known as Giardia intestinalis and Giardia duodenalis.

QIAstat-Dx Gastrointestinal Panel 2 Mini B&V: Our FDA-cleared test to analyze 4 bacterial and 1 viral target for common pathogens causing gastrointestinal symptoms using preserved stool samples (Para-Pak C&S and FecalSwab)****. 

****Results for STEC are not reported for stool specimens preserved in FecalSwab transport media.

QIAstat-Dx GI Panel 2 Mini B&V and QIAstat-Dx ME Panel are currently only available for QIAstat-Dx Analyzer 1.0.

QIAstat-Dx Meningitis/Encephalitis Panel: Our FDA-cleared test to analyze 9 bacterial, viral and fungal nucleic acids from cerebrospinal fluid specimens obtained via lumbar puncture from individuals with signs and/or symptoms of meningitis and/or encephalitis.

*****Cryptococcus neoformans and Cryptococcus gattii are not differentiated.

QIAstat-Dx GI Panel 2 Mini B&V and QIAstat-Dx ME Panel are currently only available for QIAstat-Dx Analyzer 1.0.