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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Malfunction ×

    1.3MM TI CRTX SCREW SLF-DRLG W/PLUSDRIVE(TM) RECESS 6MM

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code DZL·April 11, 2013

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code LDD·May 28, 2008

    VIRTUOSO DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code LWS·April 13, 2011

    UNKNOWN

    FDA Adverse Event
    Malfunction ·COOK, INC.·Product code DTK·August 21, 2014

    OT ULTRA2 METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·February 23, 2012

    OT ULTRA2 METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·March 18, 2011

    OT ULTRA2 METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·February 23, 2012

    GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DTK·November 1, 2017

    GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DTK·May 12, 2017

    UNKNOWN

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DTK·October 26, 2022

    GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DTK·August 24, 2016

    GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DTK·June 2, 2016