BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ASR ACETABULAR CUPS 58

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·April 23, 2013

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·April 13, 2011

    CHECK-FLO SHEATH INTRODUCER SET

    FDA Adverse Event
    Injury ·COOK, INC.·Product code DYB·July 9, 2008

    BIOMET ARCOM 3 PEG/POST

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018

    VANGUARD TIBIAL BEARING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018

    VANGUARD FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code DZI·October 6, 2020

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code DZI·July 15, 2025

    NSK

    FDA Adverse Event
    Malfunction ·NAKANISHI INC.·Product code ELC·September 9, 2016