BEUDAMED
    14 results · 22ms · Sources: EU EUDAMED, US FDA

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    LILLIPUT 1 NEW BORN HOLLOW FIBER OXYGENATOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    D901 LILLIPUT OXYGENATOR

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

    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

    EMIT QST CARBAMAZEPINE ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    ACETATE-FREE DIALYSLATE SOLUTION

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

    PROLENE POLYPROPYLENE MESH

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·February 10, 2013

    SYNCHROMED EL

    FDA Adverse Event
    Injury ·RICE CREEK MANUFACTURING·Product code LKK·January 4, 2011

    DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CALI·Product code KDI·July 23, 2014

    1.5MM SYSTEM 4 HOLE LONG STRAIGHT PLATE

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·December 12, 2017