BEUDAMED
    12 results · 20ms · 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 ×

    MULTI LEAD TRIAL CABLE

    FDA 510(k)
    FDA Class 2 ·Neurology

    PIVOX™ Oblique Lateral Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169604896·SPACER 2130545 OLIF25 27MM 0 DEG 16X45

    SurgyCut

    FDA UDI
    U.S. SURGITECH INC.·00810014635231·SurgyCut Colorado Needle with Handle Electrode ...

    SLEEPRIGHT

    FDA 510(k)
    FDA Unclassified ·Unknown

    CRP-LATEX (II)X2 SEIKEN ASSAY KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    SET, ADMINISTRATION, INTRAVASCULAR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·June 6, 2016

    FETAL MONITOR/CARDIOTOCOGRAM

    FDA Adverse Event
    Injury ·BISTOS CO., LTD.·Product code HGL·January 29, 2018

    QUATERA 700 BIMANUAL I/A HANDPIECE SET

    FDA Adverse Event
    Injury ·CARL ZEISS MEDITEC AG (OBERKOCHEN)·Product code FSO·September 8, 2023

    STOPCOCK MANIFOLD GANGS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FMG·June 17, 2020

    PROCEDURAL STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM DE MEXICO·Product code FPO·March 14, 2013

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·June 14, 2011

    SHELHI VALVE # 27

    FDA Adverse Event
    Injury ·SHELHIGH, INC.·Product code LWR·August 22, 2008