BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    ARTHREX ANGEL SYSTEM WITH ASPIRATION KIT

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code ORG·May 1, 2019

    S-ROM*HEAD FEMORAL COCR 32+0

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code JDI·October 31, 2012

    SWITCHED INTERNAL PADDLES -4.5CM

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code LDD·February 4, 2014

    FREESTYLE

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code NBW·October 9, 2007

    ACTIVE ARTICULATION HIP SYSTEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWY·October 7, 2017

    M2A-MAGNUM MODULAR HEAD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·April 6, 2017

    M2A-MAGNUM PF CUP 50ODX44ID

    FDA Adverse Event
    Injury ·.·Product code LPH·April 6, 2017

    M2A-MAGNUM PF CUP

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·October 7, 2017