BEUDAMED
    11 results · 37ms · 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 Regulation: Us FDA ×

    SECHRIST MONOPLACE HYPERBARIC OXYGEN CHAMBER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319740781·Gray Forcep, 9" (23cm) serrated

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970355·

    MODIFICATION TO UNITY NETWORK ID

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MYOSURE HYSTEROSCOPIC TISSUE REMOVAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ELEVATE SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code MAX·July 8, 2020

    BD BACTEC¿ LYTIC/10 ANAEROBIC/F CULTURE VIALS (PLASTIC)

    FDA Adverse Event
    Injury ·BECTON DICKINSON CARIBE LTD.·Product code MDB·October 11, 2021

    ASSURE 4 BLOOD GLUCOSE SYSTEM

    FDA Adverse Event
    Injury ·APEX BIOTECHNOLOGY CORP.·Product code NBW·May 31, 2013

    ALARIS PUMP MODULE ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORP.·Product code FPA·June 15, 2011

    SMART CONTROL NITINOL STENT SYSTEM

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code NIM·August 28, 2008

    CELL-DYN RUBY SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code GKZ·March 2, 2021