BEUDAMED
    255 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    TRANSPORT SERIES

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·December 7, 2012

    MAXIMO VR

    FDA Adverse Event
    Malfunction ·MEDTRONIC·Product code LWS·August 12, 2023

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM INC.·Product code MDS·April 1, 2014

    CBL 5 LEAD, SNAP, SHID, AAMI, LIMB, RGD

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·January 16, 2015

    PERMANENT PACEMAKER ELECTRODE

    FDA Adverse Event
    Malfunction ·PACESETTER·Product code DTB·August 12, 2023

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM INC·Product code MDS·March 31, 2014

    ATLAS II DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL·Product code LWS·August 11, 2023

    EON MINI

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL NEUROMODULATION, INC·Product code LGW·November 1, 2012

    ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·October 6, 2020

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·June 1, 2012

    HUDSON ET TUBE, UNCUFFED, 2.5MM

    FDA Adverse Event
    Malfunction ·TELEFLEX·Product code BTR·March 25, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·October 31, 2012

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·October 31, 2012

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM INC.·Product code MDS·April 1, 2014

    TUBE CEV649 DIA 5MM 350MM

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INSTRUMENTATION S.A.S.·Product code GEI·August 29, 2013

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 31, 2012

    DAILY ACTIVITY ASSIST DEVICE

    FDA Adverse Event
    Malfunction ·FOSHAN R. POON MEDICAL PRODUCTS CO., LTD.·Product code ILS·June 14, 2013

    ALARIS PC UNIT

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 5, 2020

    AUTOPULSE RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC·Product code DRM·March 21, 2013

    UNIVERSAL OSCILLATING SAW ATTACHMENT

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL S.A·Product code GFA·March 19, 2014