
QSG rev.3
First-time Barcode Scanner Setup
Datalogic QuickScan Barcode Wand, QD2430
The DxHub requires input from a barcode scanner. The scanner is NOT
provided with the DxLab COVID-19 Test or the DxHub and should be purchased
separately. The barcode scanner will supply a character string that appears in
the text box as if it was typed on the onscreen keyboard.
The recommended barcode scanner is the Datalogic QuickScan QD2430
(QD2430-BK or QD2430-WHfrom BarcodeFactory). The QD2430 scanner is
connected to the instrument via a specific cable supplied with the DxHub. Once
connected and set up, the scanner is typically operated in default mode and will
read both standard barcodes and 2D, QR-type barcodes.
●Plug the cable provided with the
DxHub (NOT
the cable included with
the barcode scanner) into the barcode
scanner handle. Connect the barcode
scanner cable to the DxHub rear port.
●On the DxHub touchscreen, select
the “Test” icon.
●Select “Test”.
● Select “COVID-19” test.
●Wait for the instrument to reach
66°C.
●
Select any unoccupied test bay (empty
box). #4 is highlighted for
demonstration purposes.
●Once the Sample-ID screen has
been reached, pick up the barcode
scanner.
●Using the barcode scanner, scan
the above barcode first. If scanned
successfully, the scanner will
generate a tone on the scan and
then generate a second tone
moments after.
●If two tones are not heard, refer to
the DxHub manual to troubleshoot.
●Using the barcode scanner, scan the
above barcode second. If scanned
successfully, the scanner will generate
a tone on the scan and then generate a
second tone moments after. The
barcode scanner is now ready for use.
●If two tones are not heard, refer to the
DxHub manual to troubleshoot.
●Touch ✘three times to return to
the logout screen.
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Warning
•This product has not been FDA cleared or approved, but has been authorized for emergency use by FDA under an EUA for use by authorized laboratories;
•This product has been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens; and
•The emergency use of this product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency
use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. §
360bbb-3(b)(1), unless the declaration is terminated or authorization is revoked sooner.