BEUDAMED
    7 results · 17ms · Sources: EU EUDAMED, US FDA

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    G2 X FILTER SYSTEM - FEMORAL

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·January 10, 2013

    AQUATRACK HYDROPHILIC GUIDEWIRE

    FDA Adverse Event
    Malfunction ·ARGON MEDICAL DEVICES, INC.·Product code DQX·December 6, 2010

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 18, 2014

    JAWS "HIQ+", 5 X 330 MM, GRASPING FORCEPS, CROCEOLMI

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·March 15, 2023

    JAWS "HIQ+", 5 X 330 MM, SCISSORS, METZENBAUM

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·March 30, 2023

    SHAFT "HIQ+", 5 X 330 MM

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·May 23, 2023

    JAWS "HIQ+", 5 X 330 MM, GRASPING FORCEPS, CROCEOLMI

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·March 15, 2023