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QIAstat-Dx Analyzer

Discover the QIAstat-Dx Cartridge

All-in-one mini lab that provides results in about an hour


See the assays

QIAstat-Dx Analyzer
Operational Module

The Operational Module provides connectivity to the Analytical Module and enables user interaction.

  • Saves user time during setup - simple and intuitive workflow with touchscreen
  • Easily tracks patient results - bar code reader to scan patient samples and cartridges
  • Reduces errors - USB ports and ethernet connector for assay and system upgrades, document export and printer connectivity

QIAstat-Dx Analyzer
Analytical Module

The Analytical Module provides sample to insight results with real-time PCR technology in about an hour.

  • Expands testing capacity - short turnaround time to result
  • Simplifies testing protocols - all-in-one mini lab cartridge with pre-loaded reagents
  • Delivers clear qualitative results - including Ct values and amplification curves
9-inch touchscreen
graphical user interface
Barcode reader
Operational module (OM)
Dimension (WxHxD): 234 x 326 x 517mm
Weight: 5kg
ON/OFF button
USB port
Analytical module (AM)
Dimension (WxHxD): 153 x 307 x 428mm
Weight: 16kg
Analyzer status indicator
Cartridge entrance port
Mains power connector
Cartridge entrance port
Analytical module (AM)
Dimension (WxHxD): 153 x 307 x 428mm
Weight: 16kg
Power switch
USB & Ethernet ports for HIS/LIS connectivity and printing
Operational module (OM)
Dimension (WxHxD): 234 x 326 x 517mm
Weight: 5kg
Up to 4 Analytical Modules
can be added
Power switch
Analytical module 1 (AM)
Dimension (WxHxD): 153 x 307 x 428mm
Weight: 16kg
Analytical module 2 (AM)
Dimension (WxHxD): 153 x 307 x 428mm
Weight: 16kg
Mains power connector
Operational module (OM)
Dimension (WxHxD): 234 x 326 x 517mm
Weight: 5kg

QIAstat-Dx Analyzer

Less than one minute of set-up for comprehensive results in about an hour.

Available assays

  • QIAstat-Dx Respiratory Panel
  • QIAstat-Dx Respiratory SARS-CoV-2 Panel (Emergency Use Authorization)

The QIAstat-Dx Analyzer and the QIAstat-Dx Respiratory Panel are intended for in vitro diagnostic use.

The QIAstat-Dx Respiratory SARS-CoV-2 Panel is intended for in vitro diagnostic use under Emergency Use Authorization Only. Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. §263a, to perform high complexity and moderate complexity tests.

The QIAstat-Dx Respiratory SARS-CoV-2 Panel has not been FDA cleared or approved;

The QIAstat-Dx Respiratory SARS-CoV-2 Panel has been authorized by FDA under an EUA for use by authorized laboratories;

The QIAstat-Dx Respiratory SARS-CoV-2 Panel has been authorized only for the detection and differentiation of nucleic acid of SARS-CoV-2 from multiple respiratory viral and bacterial organisms;

The QIAstat-Dx Respiratory SARS-CoV-2 Panel is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostic tests for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Act, 21 U.S.C. § 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner.


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