BEUDAMED
    522 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    CADD

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL MD, INC.·Product code FRN·October 16, 2019

    EXTENSION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FPA·March 19, 2020

    VITROS 4600 CHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code JJE·April 29, 2025

    GORE® EXCLUDER® AAA ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·December 2, 2022

    UNSPECIFIED BD DEVICE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·May 26, 2021

    ARTIS PHENO

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE GMBH-AT·Product code OWB·December 9, 2021

    GORE® EXCLUDER® CONFORMABLE AAA ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·January 3, 2023

    GORE® TAG® CONFORMABLE THORACIC STENT GRAFT WITH ACTIVE CONTROL SYSTEM

    FDA Adverse Event
    Malfunction ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·December 16, 2024

    ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·January 14, 2021

    CADD SOLIS VIP PUMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC·Product code FRN·April 14, 2025

    MAXPLUS POSITIVE PRESSURE CONNECTOR

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FPA·June 11, 2019

    WALKMED 350 VL AMBULATORY PUMP

    FDA Adverse Event
    Malfunction ·WALKMED LLC·Product code FRN·March 13, 2019

    WANDA PTA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code LIT·December 7, 2009

    VITROS 5600 INTEGRATED SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code JJE·March 5, 2025

    EVOLUT R TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO S. DE R.L. DE CV·Product code NPT·May 6, 2026

    LCA POSITIONER

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS EUROPE·Product code LCI·February 3, 2004

    SPECTRUM SERIES II

    FDA Adverse Event
    Malfunction ·ABBOTT MFG., INC.·Product code LCI·April 17, 1997

    ASSYM

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS·Product code LCI·June 24, 1997

    HYBRITECH ICON II HCG

    FDA Adverse Event
    Malfunction ·HYBRITECH CORP.·Product code LCY·March 9, 2000

    ELECSYS 2010 ANALYZER

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LCI·January 19, 2001