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 FDA Adverse Event ×

    UNKNOWN METAL COMPONENT

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·February 25, 2026

    NV GXL LNR, +5LAT, 36MM G2-52/54MM CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·February 25, 2026

    NOVATION HIP COMPONENTS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·February 25, 2026

    FOGARTY

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES PR·Product code DXE·November 27, 2024

    FOGARTY

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES PR·Product code DXE·February 4, 2026

    HEARTSTART FR3 ECG, BASIC BUNDLE, EUROPE

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·February 21, 2014

    PLUM 1.6 W/DATAPORT

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·October 18, 2012

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·May 28, 2015

    FOGARTY

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code DXE·March 13, 2025

    FOGARTY

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES, PR·Product code DXE·September 5, 2025

    FOGARTY

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code DXE·February 11, 2025