BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    Cathtong I PICC Catheter

    FDA 510(k)
    FDA Class 2 ·General Hospital

    STOCKERT AIR PURGE CONTROL SYSTEM MODEL 23-45-05

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NIPRO HUBER INFUSION, EXCEL HUBER NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    VIRTUOSO VR

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code LWS·June 8, 2013

    CONSEPT 1 STEP NEUTRALIZING TABLETS

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code LPN·October 8, 2014

    COOL PATH DUO 7F, 1304-CP2-7-1.5(5)2-M-TE4BE1AB

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, IRVINE·Product code OAD·June 21, 2011

    SMARTSET HV BONE CEMENT 40G

    FDA Adverse Event
    Injury ·DEPUY CMW - 9610921·Product code LOD·December 4, 2019

    AES-50SP PARADIGM EDGE HIP PROBE, 50 DEGREE

    FDA Adverse Event
    Injury ·CONMED UTICA·Product code GEI·May 18, 2023

    AES-50SP PARADIGM EDGE HIP PROBE, 50 DEGREE

    FDA Adverse Event
    Malfunction ·CONMED UTICA·Product code GEI·May 25, 2023

    ELEKTA LIMITED Elekta Synergy, REF MRT 8501, MRT 8511; Medical Charged-Particle Radiation Therapy System Accelerator, Linear

    FDA Enforcement
    Class II ·Ongoing·Elekta, Inc.·December 13, 2023