BEUDAMED
    11 results · 35ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Injury ×

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDC·May 17, 2017

    DISC LT DSTL HMRL BDY SET

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDC·April 1, 2019

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDC·May 17, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDC·May 19, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDC·May 19, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDC·May 17, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDC·May 19, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDC·May 17, 2017

    XIENCE SKYPOINT¿

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR INC.·Product code NIQ·August 25, 2025

    HAP MODULAR TAPERLOC FEMORAL 7.5MM X 135MM LATERALIZED STEM/POROUS COATED

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·August 16, 2012

    M2A MAGNUM MODULAR HEAD 50MM HEAD DIAMETER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·August 16, 2012