BEUDAMED
    2,330 results · 39ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    VALIANT CAPTIVIA UNK

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code MIH·August 13, 2020

    NEOBLUE 3 LED PHOTOTHERAPY SYSTEM

    FDA Adverse Event
    Malfunction ·NATUS MEDICAL INCORPORATED·Product code LBI·January 30, 2018

    NEOBLUE MINI LED PHOTOTHERAPY SYSTEM

    FDA Adverse Event
    Malfunction ·NATUS MEDICAL INCORPORATED·Product code LBI·January 30, 2018

    NOKIA LUMIA 1020 (GOCHECK KIDS MOBILE APP INSTALLED) PRODUCT CODE INCORRECT N/A

    FDA Adverse Event
    Malfunction ·ORIGINAL MANUFACTURER NOKIA OUT OF BUSINESS·Product code HLM·September 12, 2018

    SCREWDRIVER BIHEX Ø3 W/T-HANDLE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HXX·January 22, 2013

    SCREWDRIVER BIHEX Ø3 W/T-HANDLE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HXX·June 23, 2013

    SCREWDRIVER BIHEX Ø3 W/T-HANDLE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HXX·June 23, 2013

    SCREWDRIVER BIHEX Ø3 W/T-HANDLE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HXX·June 18, 2013

    SCREWDRIVER BIHEX Ø3 W/T-HANDLE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWC·November 16, 2012

    CERCLWIRE Ø1 W/EYE L600 SST

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code LRN·December 28, 2012

    SCREWDRIVER BIHEX Ø3 W/T-HANDLE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HXX·September 5, 2013

    SCREWDRIVER BIHEX Ø3 W/T-HANDLE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HXX·July 22, 2013

    SCREWDRIVER BIHEX Ø3 W/T-HANDLE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HXX·December 30, 2013

    SCR-DRIVER-HEX Ø3 W/T-HANDLE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HXX·June 27, 2013

    STERNAL CABLE Ø1 W/NEEDLE+FIXATION SLEEV

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code JDQ·November 26, 2013

    STERNAL CABLE Ø1 W/NEEDLE+FIXATION SLEEV

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code JDQ·November 26, 2013

    STERNAL CABLE Ø1 W/NEEDLE+FIXATION SLEEV

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HRS·November 26, 2013

    STERNAL CABLE Ø1 W/NEEDLE+FIXATION SLEEV

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code JDQ·November 26, 2013

    DRILL BIT Ø2 W/MARKING L110/85 2FLUTE

    FDA Adverse Event
    Malfunction ·OBERDORF : SYNTHES PRODUKTIONS GMBH·Product code GFG·December 7, 2017

    K-WIRE Ø2 W/DOUB TIP L150 SST

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code LRN·February 4, 2013