BEUDAMED
    87 results · 65ms · Sources: EU EUDAMED, US FDA

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    CLEAR CARE

    FDA Adverse Event
    Injury ·Product code LPN·October 26, 2015

    INTELLIVUE MX40 2.4GHZ

    FDA Adverse Event
    Injury ·PHILIPS MEDICAL SYSTEMS·Product code MHX·November 7, 2025

    30 ML BD LUER-LOK¿ TIP SYRINGE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMF·August 31, 2022

    HEARTMATE 3 LVAS IMPLANT KIT

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·October 11, 2023

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·July 8, 2009

    CLEAR CARE PLUS HYDRAGLYDE

    FDA Adverse Event
    CIBA VISION CORPORATION/ALCON LABORATORIES, INC.·Product code LPN·July 13, 2020

    JUVEDERM VOLUMA XC/LIDO (VOLUME UNKNOWN)

    FDA Adverse Event
    Injury ·ALLERGAN (PRINGY)·Product code LMH·October 20, 2022

    ZIP CLOSURE WITH POUCH

    FDA Adverse Event
    Malfunction ·MEDICAL ACTION INDUSTRIES, INC.·Product code LIO·January 4, 2012

    ZIP CLOSURE WITH POUCH

    FDA Adverse Event
    Malfunction ·MEDICAL ACTION INDUSTRIES, INC.·Product code NNI·September 21, 2011

    OT SELECT SIMPLE METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 27, 2017

    OT SELECT SIMPLE METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE GMBH·Product code NBW·February 4, 2019

    OT VERIO IQ METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 4, 2016

    OT VERIO IQ METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 30, 2016

    CLEAR CARE

    FDA Adverse Event
    Injury ·Product code LPN·December 12, 2012

    MW5057433

    FDA Adverse Event
    Injury ·October 26, 2015

    OT SELECT SIMPLE METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 27, 2017

    NOVOPEN 4

    FDA Adverse Event
    Injury ·NOVO NORDISK A/S, MEDICAL SYSTEMS·Product code FMF·July 1, 2022

    NOVOPEN 4

    FDA Adverse Event
    Injury ·NOVO NORDISK A/S, MEDICAL SYSTEMS·Product code FMF·August 23, 2022

    PLUM A+ DRIVER EDITI

    FDA Adverse Event
    Injury ·HOSPIRA HOLDINGS DE COSTA RICA LTD.·Product code FRN·March 15, 2013

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·April 6, 2016