BEUDAMED
    37 results · 61ms · Sources: EU EUDAMED, US FDA

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    ELECSYS HIV DUO REAGENT PACK

    FDA Adverse Event
    Malfunction ·ROCHE MOLECULAR SYSTEMS, INC.·Product code MZF·December 22, 2022

    WATCHMAN FLX? PRO

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NGV·October 30, 2025

    WATCHMAN FLX? PRO

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NGV·August 29, 2025

    DUETT PRO SEALING DEVICE

    FDA Adverse Event
    Death ·VASCULAR SOLUTIONS, INC.·Product code MGB·June 20, 2003

    ELECSYS HIV DUO

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code MZF·January 13, 2026

    WATCHMAN FLX PRO

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NGV·December 12, 2024

    ELECSYS TROPONIN T HS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code MMI·August 27, 2025

    UNICEL DXC 600 PRO SYNCHRON SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code JJE·May 12, 2016

    UNICEL DXI 800 ACCESS IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Other ·BECKMAN COULTER, INC.·Product code MMI·December 24, 2008

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·October 11, 2018

    WATCHMAN FLX? PRO

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NGV·June 12, 2025

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·October 31, 2018

    WATCHMAN FLX? PRO

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NGV·July 28, 2025

    UNICEL® DXL 600 ACCESS® IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code MMI·August 13, 2009

    IMMULITE 2000

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code NBC·December 9, 2011

    XIENCE PRO EVEROLIMUS ELUTING RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·March 4, 2014

    WATCHMAN FLX PRO

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NGV·December 13, 2024

    CATHETER ACUNAV DIAGNOSTIC ULTRASOUND 8FR FOR USE WITH SIEMENS SYSTEM

    FDA Adverse Event
    Malfunction ·STERILMED, INC.·Product code OWQ·May 5, 2023

    WATCHMAN FLX? PRO

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NGV·September 20, 2024

    HEARTWARE VENTRICULAR ASSIST SYSTEM - PUMP/DRIVELINE

    FDA Adverse Event
    Injury ·HEARTWARE, INC.·Product code DSQ·July 21, 2021