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10/11/2026 09:05
Cepheid Achieves CE Marking Under IVDR for Xpert® Respiratory PanelEQS-News: Cepheid / Key word(s): ESG/Contract IVDR-compliant PCR test detects 13 common respiratory pathogens from a single sample. SUNNYVALE, Calif., Nov. 10, 2026 /PRNewswire/ -- Cepheid, a Danaher company, announced today that it has achieved CE marking under the in vitro medical device regulation (IVDR) for the Xpert Respiratory Panel, a multiplex PCR test designed to detect 13 common viral and bacterial respiratory pathogens from a single nasopharyngeal swab sample. The test is intended to aid in the diagnosis of suspected infectious respiratory tract infection, in conjunction with other clinicopathological factors.
Respiratory Infections Pose Diagnostic Challenges Children, older adults, and immunocompromised individuals are at increased risk for complications from respiratory infections and may require hospitalization.⁴ Additionally, specific viral infections and bacterial co-infections are associated with increased disease severity and adverse outcomes,4 reinforcing the importance of distinguishing the underlying pathogens to help inform clinical assessment. Advancing Diagnostic Excellence, Supporting Diagnostic Stewardship Cepheid's respiratory portfolio enables healthcare organizations to deploy diagnostic excellence by enabling healthcare organizations to implement diagnostic stewardship strategies on a single GeneXpert system. From targeted testing to broad syndromic respiratory panels, clinicians can select the right test for the right patient at the right time, supporting patient stratification, workflow efficiency, and more effective utilization of healthcare resources.5 Multiplex Molecular Testing Impact "As healthcare systems across Europe prepare for the upcoming respiratory season, the ability to match the right test to the right patient is more important than ever," said Christoph Martinaud, Senior Director, Medical Affairs EMEA at Cepheid. "The Xpert Respiratory Panel further strengthens Cepheid's respiratory portfolio, enabling clinicians to choose from targeted single-pathogen tests, mid-plex panels, or broader syndromic respiratory panels on the same GeneXpert system. This clearance reflects our commitment to continuously accelerate ideas to impact, bringing meaningful diagnostic innovations to providers and patients." Compatible with GeneXpert® Systems The Xpert Respiratory Panel maintains the simplicity of existing workflows, requiring less than one minute of hands-on time while providing on-demand answers. The test will begin shipping to countries accepting the CE mark in the coming weeks. For more information about the Xpert Respiratory Panel and Cepheid's full menu of molecular diagnostic solutions, visit www.cepheid.com. CE-IVD. In Vitro Diagnostic Medical Device. References
About Cepheid About Danaher For Cepheid Media Inquiries:
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