BEUDAMED
    202 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 ×

    SYNCHRONY

    FDA Adverse Event
    Malfunction ·MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH·Product code MCM·October 22, 2024

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·January 25, 2018

    RELAY THORACIC STENT-GRAFT WITH PLUS DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·BOLTON MEDICAL, INC.·Product code MIH·June 3, 2022

    RESTORE ADVANCED

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·October 25, 2013

    REAMER 0ZZ F/PFNA BLADE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTO·October 5, 2012

    TERUMO CARDIOVASCULAR PROCEDURE KIT

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code OEZ·August 7, 2017

    SX OXYGENATOR W/ X COATING

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code DTZ·March 2, 2016

    CARDIOVASCULAR PROCEDURE KIT

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code OEZ·August 8, 2024

    SX OXYGENATOR W/ X COATING

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code DTZ·March 2, 2016

    CAPIOX FX ADVANCE HOLLOW FIBER OXYGENATOR W INTEGRATED AF W HARDSHELL RES.

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code DTZ·December 20, 2024

    CAPIOX FX OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·April 18, 2013

    CAPIOX FX 15 HOLLOW FIBER OXYGENATOR AF

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·August 12, 2016

    160-R SKINMARKER REGULAR

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FZZ·December 6, 2016

    RICHARD-ALLAN REGULAR TIP PEN W/ RULER

    FDA Adverse Event
    Malfunction ·ASPEN SURGICAL PRODUCTS, CALEDONIA·Product code FZZ·November 22, 2016

    COMPAX 40E

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code IZZ·March 30, 2009

    COMPAX 400

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS S.C.S.·Product code IZZ·January 11, 2009

    COMPAX 40E

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code IZZ·January 13, 2009

    CODMAN SURGICAL MARKER

    FDA Adverse Event
    Malfunction ·CODMAN & SHURTLEFF·Product code FZZ·May 14, 2014

    NS-151 FINE TIP SKIN MARKER

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FZZ·November 15, 2016

    RICHARD-ALLAN REGULAR TIP PEN W/ RULER

    FDA Adverse Event
    Malfunction ·ASPEN SURGICAL PRODUCTS, CALEDONIA·Product code FZZ·October 31, 2016