BEUDAMED
    6 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    QUIK-COMBO PACING/DEFIBRILLATION/ECG

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL CORP·Product code LDD·March 31, 1998

    IMP,1-PC,ANG,3.0X13MM

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·September 19, 2024

    IMP,1-PC,ANG,3.0X13MM

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·October 11, 2019

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·April 11, 2013

    BIPHASIC LIFEPAK(R) 500 AUTOMATED EXTERNAL DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·September 2, 2014

    S-ROM M HEAD 36MM +9

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·April 7, 2011