QIAGEN receives U.S. clearance for second QIAstat-Dx mini gastrointestinal panel, expanding U.S. syndromic testing portfolio (QIAGEN)

QIAGEN has received FDA clearance for its QIAstat-Dx Gastrointestinal Panel 2 Mini B, expanding its U.S. syndromic testing portfolio for gastrointestinal infections. The panel rapidly detects five key bacterial pathogens—Campylobacter, Salmonella, STEC, Shigella, and Yersinia enterocolitica—in about one hour, supporting fast outpatient diagnostics. This is QIAGEN’s second FDA-cleared QIAstat-Dx panel in 2025 and complements their existing bacterial and viral GI panels, offering laboratories targeted, flexible solutions for diverse clinical settings.