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

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    KARL STORZ XENON LIGHT SOURCE MODEL 201320-20

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    QUALTEX SKIN MARKER

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    DELUXE WALL-MOUNTED CEPHALOMETER

    FDA 510(k)
    FDA Class 1 ·Radiology

    V18 CONTROL WIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP·Product code DQX·March 16, 2007

    V18 CONTROL WIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DQX·May 23, 2007

    9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 10, 2013

    EON IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·November 23, 2010

    LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR

    FDA Adverse Event
    Injury ·PHYSIO-CONTROL, INC·Product code MKJ·July 15, 2014