BEUDAMED
    11 results · 30ms · Sources: EU EUDAMED, US FDA

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    neuro inspire

    FDA 510(k)
    FDA Class 2 ·Neurology

    Biomet® Hip System

    FDA UDI
    Biomet Orthopedics, LLC·00887868308307·

    BIOMET HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·05019279400768·

    LANX LATERAL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SHARPS CONTAINER, MODEL 039-413

    FDA 510(k)
    FDA Class 2 ·General Hospital

    HANDLE BATTERY POWERED DRIVER

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWE·March 4, 2025

    HEARTMATE II LVAS IMPLANT KIT (WITH SEALED GRAFTS)

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·November 4, 2022

    SUPER POLIGRIP

    FDA Adverse Event
    Other ·GLAXOSMITHKLINE·Product code KOL·June 13, 2011

    ACCESS® 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code JJE·June 11, 2013

    ASCENSIA CONTOUR

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·September 9, 2008

    BD DISCARDIT¿ II SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·December 6, 2018