BEUDAMED
    15 results · 24ms · Sources: EU EUDAMED, US FDA

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    IAMIN GEL WOUND DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    TECHNICON CHEM 1 SYS ANALYTES MAGNESIUM GGT, URIC

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    RAPITEX (R) CRP NEW

    FDA 510(k)
    FDA Class 2 ·Immunology

    D901 LILLIPUT OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·October 13, 2021

    UNK IVS TUNNELLER DEVICE

    FDA Adverse Event
    Injury ·BALLYMONEY - USS·Product code FTL·January 31, 2013

    RESTORE RECHARGABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·January 4, 2011

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 23, 2014

    CUSTOM PERFUSION PACK

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·October 30, 2012

    LILLIPUT 1 START

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·April 17, 2023

    ALP 501

    FDA Adverse Event
    Injury ·CURRIE MEDICAL SPECIALTIES·Product code JOW·September 1, 2012

    LILLIPUT 1 OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALY·Product code DTZ·December 27, 2024

    LILLIPUT 1 NEW BORN HOLLOW FIBER OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·December 6, 2024

    LILLIPUT 1 NEW BORN HOLLOW FIBER OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·January 17, 2022

    LILLIPUT 1 NEW BORN HOLLOW FIBER OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·January 25, 2022

    ALP 501

    FDA Adverse Event
    Injury ·CURRIE MEDICAL SPECIALTIES·Product code JOW·July 25, 2012