BEUDAMED
    19 results · 23ms · Sources: EU EUDAMED, US FDA

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    BD INSULIN SYRINGE W/ BD ULTRA-FINE NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·August 8, 2019

    SYRINGE 0.3ML 31GA 6MM HALFUNIT

    FDA Adverse Event
    Injury ·BD MEDICAL - DIABETES CARE·Product code FMF·May 1, 2020

    ASR ACETABULAR CUPS 58

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·April 11, 2012

    BD INSULIN SYRINGE WITH BD ULTRA-FINE NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·March 10, 2020

    BD SYRINGE 0.3ML 31GA 6MM HALFUNIT

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·December 19, 2019

    E-CAM COINCIDENCE MODE [510 (K) K970627)

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SYSTEMS, INC., NMG GROUP·Product code IYX·April 20, 2001

    ASR ACETABULAR CUPS 48

    FDA Adverse Event
    Injury ·DEPUY INTL, LTD.·Product code KWA·December 29, 2010

    CANNULATED CRUCIFORM SCREWDRIVER

    FDA Adverse Event
    Malfunction ·SYNTHES BRANDYWINE·Product code HXX·April 22, 2013

    FLOSEAL HEMOSTATIC MATRIX

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - HAYWARD·Product code LMF·April 27, 2011

    ADV BASIC SYSTEM, UC/MOB, DOM

    FDA Adverse Event
    Malfunction ·LIEBEL-FLARSHEIM CO.·Product code DXT·July 1, 2008

    ASR UNI FEMORAL IMPL SIZE 51

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·August 21, 2013

    ASR ACETABULAR CUPS 60

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·October 24, 2015

    ASR ACETABULAR CUPS 58

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·August 21, 2013

    ASR UNI FEMORAL IMPL SIZE 49

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·July 22, 2013

    ADAPTER SLEEVES 12/14 +8

    FDA Adverse Event
    Injury ·DEPUY INTL.,LTD 8010379·Product code KWA·November 4, 2015

    KYPHON KURVE BONE FILLER DEVICE 13GA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code KIH·July 14, 2020

    ADAPTER SLEEVES

    FDA Adverse Event
    Injury ·DEPUY INTL.,LTD 8010379·Product code KWA·February 2, 2016

    ASR ACETABULAR CUPS 56

    FDA Adverse Event
    Injury ·DEPUY INTL.,LTD 8010379·Product code KWA·February 2, 2016

    ASR UNI FEMORAL IMPL SIZE 53

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·October 23, 2015