BEUDAMED
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    DIACAM (510(K) K 901019)

    FDA Adverse Event
    Other ·SIEMENS MEDICAL SYSTEMS·Product code KPS·March 13, 2001

    PRODUCT CODE 901012 PARA-PAK ZN-PVA

    FDA Adverse Event
    Other ·MERIDIAN BIOSCIENCE, INC.·Product code JSM·September 10, 2004

    PRODUCT CODE 901012 PARA-PAK ZN-PVA

    FDA Adverse Event
    Other ·MERIDIAN BIOSCIENCE, INC.·Product code LDX·September 9, 2004

    ADVIA CENTAUR XP

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code MMI·June 30, 2014

    RESOLUTION CLIP CLIPPING DEVICE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code MND·January 8, 2013

    RESOLUTION HEMOSTASIS CLIPPING DEVICE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code MND·November 17, 2010

    INTELLIS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·May 7, 2025