BEUDAMED
    16 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    RINGLOC HIP SYSTEM ACETABULAR BI-POLAR CUP

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code JDI·June 15, 2017

    E1 RINGLOC BIPOLAR 28X43MM

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code HBE·June 22, 2016

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·April 10, 2013

    E1 RINGLOC BIPOLAR 28X50MM

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code JDI·May 2, 2018

    RINGLOC HIP SYSTEM ACETABULAR BIPOLAR CUP

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code JDI·January 6, 2017

    E1 RINGLOC BIPOLAR 28X47MM

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code JDI·May 3, 2017

    RINGLOC BIPOLAR VIT E 28X44MM

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·February 18, 2025

    E1 RINGLOC BIPOLAR 28X51MM

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code JDI·October 26, 2020

    E1 RINGLOC BIPOLAR 28X52MM

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code JDI·February 14, 2021

    RINGLOC HIP SYSTEM

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code JDI·March 20, 2017

    BI-POLAR ACETABULAR CUP

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code JDI·February 9, 2017

    RINGLOC BIPOLAR HIP SYSTEM

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code JDI·May 19, 2025

    RINGLOC HIP SYSTEM ACETABULAR BI-POLAR CUP

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code JDI·June 16, 2017

    SYNFRAME UNI-HOLDER INSULATED F/OR TABLE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code LXH·July 29, 2025

    BD MAXPLUS¿ PRESSURE RATED EXTENSION SET WITH REMOVABLE NEEDLELESS CONNECTOR

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·January 3, 2023

    BD MAXPLUS¿ PRESSURE RATED EXTENSION SET WITH REMOVABLE NEEDLELESS CONNECTOR

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·January 3, 2023