BEUDAMED
    14 results · 37ms · Sources: EU EUDAMED, US FDA

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    THE ELEVENTH FINGER

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111079·SILICONE MAT FOR K 9-2330

    DEVEX MESH SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    2008 HEMODIALYSIS SORBENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    D901 LILLIPUT OXYGENATOR

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

    SROM 28MM +6 M HEAD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code JDI·December 8, 2010

    ARTICULEZE M HEAD 36MM +5

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD.·Product code JDI·January 22, 2013

    SUSTAIN XL SRP

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·July 9, 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

    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