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QIAGEN Expands US QIAstat-Dx Portfolio With New FDA-Cleared Panel

Published

2 October 2026

Topic

opportunities

◆ Sectors

Diagnostics

◆ Geography

United States

◆ Source

Read at es.tradingview.com →

◆ Verified

Fusion42 · 3 October 2026 · Fusion42 review

QIAGEN received FDA clearance for its new QIAstat-Dx BCID GN Plus AMR Panel, expanding rapid bloodstream infection testing in the US to cover key gram-negative bacteria and antibiotic resistance markers, complementing its existing gram-positive and fungal panel.

This Wire brief sits within Fusion42's coverage of Diagnostics.

◆ ◆ The Wire takeaway

You can now offer US labs a broader rapid test that identifies crucial gram-negative bacteria and resistance markers within an hour. Rapid infectious disease diagnostics just opened a new door for labs and treatment decision tools, speeding critical care.

◆ Coverage

1 source · 2 Oct 2026

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◆ Topics

DiagnosticsFDA-clearancebloodstream-infectionrapid-diagnosticsantimicrobial-resistanceQIAstat-Dx