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QIAstat-Dx Analzyer and QIAstat-Dx Rise features
With the QIAstat-Dx family of analyzers, we have an instrument for every lab. Regardless of the configuration, all analyzers have modular options allowing for customization for your lab. And they all run assays using our preloaded cartridges and intuitive touchscreen display.
QIAstat-Dx Analyzer and QIAstat-Dx Rise specifications
Discover the assay menu
All QIAstat-Dx panels harness the power of our sleek cartridge design. This technology redefines ease-of use for multiplex testing by creating a workflow with less than one minute hands-on time.
- Save time – all reagents are preloaded into the cartridge
- Reduce errors and risk of contamination – tests are performed on a single instrument solution
- Lower costs – cartridges are shipped and stored at room temperature
QIAstat Respiratory SARS-CoV-2 Panel
This expanded version of our multiplex respiratory cartridge detects and differentiates† 22 viral and bacterial respiratory targets, including SARS-CoV-2 to support efforts to provide accessible testing to meet the demands of the COVID-19 outbreak.
QIAstat-Dx Gastrointestinal Panel 2
New! With this updated version of our CE-marked gastrointestinal panel, differentiate STEC toxins stx1 and stx2.
Detect and differentiate 22 viral, bacterial and parasitic pathogens in patients with suspected gastrointestinal infections.
This panel runs on both the QIAstat-Dx Analyzer and QIAstat-Dx Rise.
QIAstat-Dx Meningitis/Encephalitis Panel
Our QIAstat-Dx Meningitis/Encephalitis Panel provides comprehensive results in about an hour, ensuring the most serious infections won’t go missed.
Detect and differentiate 15 viral, bacterial and fungal pathogens in patients with suspected central nervous system infections.
This panel runs on the QIAstat-Dx Analyzer.
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*Some features require a QIAstat-Dx Connectivity plan. Flexible plans are available to meet your lab’s needs.
The QIAstat-Dx Analyzer, QIAstat-Dx Rise and QIAstat-Dx panels are intended for in vitro diagnostic use.
The QIAstat-Dx ME Panel is indicated as an aid in the diagnosis of specific agents that cause meningitis and/or encephalitis, and results must be used in conjunction with other clinical, epidemiological, and laboratory data. Results from the QIAstat-Dx ME Panel are not intended to be used as the sole basis for diagnosis, treatment, or other patient management decisions. Positive results do not rule out co-infection with organisms not included in the QIAstat-Dx ME Panel. The agent or agents detected may not be the definite cause of the disease. Negative results do not preclude central nervous system (CNS) infection.
The QIAstat-Dx ME Panel is intended for in vitro diagnostic use by laboratory professionals only.
Product availability may differ from country to country based on regulations and approvals. Contact your country representative for further details.