BEUDAMED
    10 results · 26ms · Sources: EU EUDAMED, US FDA

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    IL TEST D-DIMER

    FDA 510(k)
    FDA Class 2 ·Hematology

    FORZA® XP Expandable Spacer System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ANT ANGIOGRAPHIC SYRINGES, MODEL(S) 100101,102,103,100201,202,203,204,100301,200101,201,202, 203,200301,101,102,202,301

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    IBP ELBOW INTERLOK FINISH ULNAR COMPONENT STANDARD LEFT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDB·June 14, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDB·February 9, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDB·March 2, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDB·February 9, 2017

    EVERCROSS¿ .035" OTW PTA DILATATION CATHETER

    FDA Adverse Event
    Injury ·EV3 INC.·Product code DQY·February 21, 2013

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·January 20, 2011

    S-ROM M HEAD 36MM +3

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code JDI·August 1, 2014