Aviso: Este sitio agrega datos públicos oficiales de la FDA, ClinicalTrials.gov, PubMed y SEC EDGAR solo como referencia general. No constituye asesoramiento médico, diagnóstico, recomendaciones de tratamiento ni asesoramiento de inversión.

PubMed

Device failures and patient adverse events from EUS: 26-year FDA MAUDE analysis (2000-2025).

PMID: 41938148 ·

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RevistaEndoscopic ultrasound
Año
PMID41938148

Resumen

EUS has emerged as an essential instrument in the field of gastroenterology, significantly enhancing both diagnostic evaluations and therapeutic procedures. By delivering high-resolution imaging and precise guidance, EUS facilitates a range of interventional techniques. This study sought to examine the adverse events linked to EUS devices following their approval by the US Food and Drug Administration. We performed a retrospective analysis utilizing postmarketing surveillance data sourced from t

Fuente oficial

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