QIAstat-Dx Rise

For higher throughput multiplex syndromic testing applications

S_1174_0_QIAstatDx_Rise_5584

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QIAstat-Dx Rise Base

Cat. No. / ID:  9003163

The QIAstat-Dx Rise Base is a benchtop in vitro diagnostic device for use with QIAstat-Dx assays and QIAstat-Dx Analytical Modules. It provides full automation from sample preparation to real-time PCR detection. This higher-throughput system can accommodate up to 160 patient samples per day using 8 Analytical Modules.
InstrumentPanel
QIAstat-Dx Rise Base
QIAstat-Dx Respiratory SARS-CoV-2 Panel
QIAstat-Dx Gastrointestinal Panel 2
QIAstat-Dx instruments and QIAstat-Dx panels are intended for in vitro diagnostic use. For up-to-date licensing information and product-specific disclaimers, see the respective QIAGEN kit instructions for use or user manual. QIAGEN instructions for use and user manuals are available at www.qiagen.com or can be requested from QIAGEN Technical Services (or your local distributor).

✓ 24/7 automatic processing of online orders

✓ Knowledgeable and professional Product & Technical Support

✓ Fast and reliable (re)-ordering

Features

  • Uses real-time PCR to deliver comprehensive results for up to 160 patient samples per day with 8 Analytical Modules
  • Easily view Ct values and amplification curves for all detected pathogens
  • Single-step cartridge preparation with no precision pipetting required and unique direct swab protocol
  • Load the full capacity of cartridges in just a few minutes and safely dispose of all used cartridges from the waste tray in one quick step

 

 

Product Details

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 one of our intuitive QIAstat-Dx instruments. 


QIAstat-Dx Rise is our higher-throughput powerhouse, built to fit the needs of high-demand institutions. Combined with QIAstat-Dx assay cartridges, QIAstat-Dx Rise uses multiplex 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. The system includes random access and batch testing options, with a daily capacity of 160 samples using 8 Analytical Modules. The QIAstat-Dx Rise also includes a multi-test front drawer that can accommodate up to 18 cartridges at the same time, and a waste drawer to automatically collect used cartridges.


Each instrument is made up of two components: 1) A QIAstat-Dx Rise Base, which contains the intuitive touch-screen interface and robotic system that moves and scans the cartridges within the device and 2) Between 1 through 8 Analytical Modules, letting you test up to eight samples at once. 

With QIAstat-Dx Rise in your lab, you can: 

  • Gain time away from your instruments: Batch process up to 16 cartridges using 8 Analytical modules.
  • Process priority tests fast: Get random access through 2 additional urgent testing slots. 
  • Load and go: Load the full capacity of cartridges in just a few minutes and safely dispose of used tests in one step.

Plus, every QIAstat-Dx Analytical Module is compatible with both QIAstat-Dx Analyzer 2.0 and QIAstat-Dx Rise. Easily update your QIAstat-Dx testing format based on your evolving testing needs. Click here to more about QIAstat-Dx Analyzer 2.0, our modular system perfect for labs of every size.

 

Principle

QIAstat-Dx Rise, combined with QIAstat-Dx assay cartridges, uses real-time PCR to detect pathogen nucleic acids in human biological samples. The instrument and cartridges are designed as a closed system that contain on board 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.

Procedure

Preparing a QIAstat-Dx cartridge using liquid transfer or dry swab sample application is efficient and fast. And once the cartridges are ready, it takes just a few minutes to load the full capacity of cartridges and start a run on QIAstat-Dx Rise. 

Loading a sample into the QIAstat-Dx cartridge requires less than one minute hands-on time with no precision pipetting.

Using the provided transfer pipette, the user applies a liquid sample to the main port of the QIAstat-Dx cartridge (see  Applying a liquid sample to the QIAstat-Dx cartridge). Alternatively for our respiratory assay, a dry swab sample may be directly applied to the cartridge ( Applying a dry swab to the QIAstat-Dx cartridge).

Following the instructions on the QIAstat-Dx Rise touchscreen display, the user loads the prepared cartridges into the instrument’s loading tray (see  Adding cartridges to the QIAstat-Dx Rise input tray).

The QIAstat-Dx Rise will automatically scan the sample ID and cartridge barcodes, or the user can manually scan the barcodes. Once the user starts the run, the QIAstat-Dx Rise will autonomously process the samples. 

The input tray also offers random and continuous access, meaning an urgent test can be added to an ongoing run at a moment’s notice. 

Once the run is finished, the used cartridges are automatically placed in the dedicated waste tray so they can be disposed of safely and quickly.

 

See figures

Applications

QIAstat-Dx Respiratory SARS-CoV-2 Panel (V2): Qualitative test to analyze 23 viral and bacterial respiratory targets for common pathogens causing respiratory infections, including SARS-CoV-2.

 

QIAstat-Dx Respiratory SARS-CoV-2 Panel (V2) – 23 bacterial and viral pathogens
Viruses   Bacteria
Influenza A Parainfluenza virus 1  
Influenza A subtype H1N1/2009 Parainfluenza virus 2  
Influenza A subtype H1 Parainfluenza virus 3  
Influenza A subtype H3 Parainfluenza virus 4 Mycoplasma pneumoniae
Influenza B Respiratory syncytial virus A/B Legionella pneumophilia
Coronavirus 229E Human metapneumovirus A/B Bordetella pertussis
Coronavirus HKU1 Adenovirus Chlamydophila pneumoniae
Coronavirus NL63 Bocavirus  
Coronavirus OC43 Rhinovirus/Enterovirus*  
SARS-CoV-2    

*Enterovirus and Rhinovirus are both detected, but not differentiated, with the QIAstat-Dx Respiratory SARS-CoV-2 Panel.

The QIAstat-Dx Respiratory SARS-CoV-Panel (V2) is currently available in select countries.

 

QIAstat-Dx Gastrointestinal Panel 2: Qualitative test to analyze 22 of the most common pathogens causing gastrointestinal infections, including differentiation of Shiga-like toxin producing E. coli (STEC) stx1 and stx2.

QIAstat-Dx Gastrointestinal Panel 2 – 23 targets, corresponding to 22 bacterial, viral and parasitic pathogens
Bacteria   Viruses Parasites
Campylobacter (C. jejuni, C. upsaliensis, C. coli) Salmonella spp. Adenovirus F40/41 Cryptosporidium
Clostridium difficile (toxin A/B) Shiga-like toxin-producing E. coli (STEC) stx1 and stx2 (including specific identification of E. coli O157 serogroup within STEC)** Astrovirus Cyclospora cayetanensis
Enteroaggregative E. coli (EAEC) Vibrio vulnificus Norovirus (GI, GII) Entamoeba histolytica
Shigella/Enteroinvasive E. coli (EIEC) Vibrio parahaemolyticus Rotavirus A Giardia lamblia
Enteropathogenic E. coli (EPEC) Vibrio cholerae Sapovirus (GI, GII, GIV, GV)  
Enterotoxigenic E. coli (ETEC) lt/st Yersinia enterocolitica    
Plesiomonas shigelloides      

**The stx1 and stx2 toxin genes of STEC are reported separately by the QIAstat-Dx Gastrointestinal Panel 2.

 

Features Specifications
Configuration Modular syndromic testing system with QIAstat-Dx Rise Base, up to 8 QIAstat-Dx Analytical Modules and 1 QIAstat-Dx Rise Mobile Table (optional).
Instrument dimensions (WxHxD) QIAstat-Dx Rise Base (door closed): 580 x 1280 x 810 mm (22.8 x 50.4 x 31.9 in) 
QIAstat-Dx Rise Base (door open): 1500 mm x 1280 x 810 mm (59 x 50.4 x 31.9 in)
For installation and service interventions, 1.5 m of space around the instrument is required.
Weight QIAstat-Dx Rise Base: 130 kg
QIAstat-Dx Analytical Module: 16 kg
QIAstat-Dx Rise Mobile Table (load-bearing capacity): 300 kg
Power requirements 200–240 VAC
Recommended clearance Left side: 80 cm
Top: 32 cm
Front: 140 cm
Operating conditions Specifications
Air temperature 15–28 ̊C
Relative humidity 20–80%
Altitude 0–2200 m
Place of operation Laboratory (inside)

 

Supporting data and figures

Resources

Safety Data Sheets (1)
Certificates of Analysis (1)