BEUDAMED
    1,887 results · 43ms · Sources: EU EUDAMED, US FDA

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    HEARTMATE II SYSTEM CONTROLLER, EU

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·April 3, 2023

    HEARTMATE 3 VAD MODULAR CABLE

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·April 18, 2023

    THORATEC® HEARTMATE 3¿ SYSTEM CONTROLLER

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·May 2, 2025

    BIOMET MODULAR TIBIAL SYSTEM -POLISHED FINNED TIBIAL TRAY 71 MM

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code KRO·February 21, 2018

    CATH LAB TRAY 836

    FDA Adverse Event
    Malfunction ·MEX03 MEXICO-JUAREZ PRESOURCE·Product code LRO·November 6, 2020

    4190 FCL S&N EP-1/POWER -NS

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code HRX·November 3, 2014

    THORATEC® HEARTMATE®, LVAS IMPLANT KIT (WITH SEALED GRAFTS)

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·March 12, 2024

    THORATEC® HEARTMATE II®, SYSTEM CONTROLLER

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·March 12, 2024

    HEARTMATE POWER MODULE PATIENT CABLE, 14 VOLT

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·February 16, 2024

    VENTED MICRO VOL.INLET, N/S

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code LHI·December 12, 2023

    BAXA EXACTAMIX 2400 COMPOUNDER VALVE SET

    FDA Adverse Event
    Malfunction ·BAXA / BAXTER HEALTHCARE CORPORATION·Product code NEP·June 14, 2022

    M2A-MAGNUM PF CUP 48ODX42ID

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code KWA·May 12, 2017

    UNIVERSAL RINGLOC 2-HOLE SHELL

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·May 22, 2017

    CER OPTION TYPE 1 TPR SLEVE -3 PE 1

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code LZO·May 12, 2017

    TI LOW PROFILE SCREW 6.5X25MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·September 28, 2017

    TPRLC 133 FP TYPE1 PPS SO 6.0

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code JDI·May 12, 2017

    DELTA CERAMIC OPTION HEAD DIA2 8

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code LZO·May 12, 2017

    TI LOW PROFILE SCREW 6.5X20MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·September 28, 2017

    TI LOW PROFILE SCREW 6.5X25MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·September 28, 2017

    R/B RLOC LHOLE SHL 50MM SZ 23

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·September 28, 2017