BEUDAMED
    14 results · 29ms · Sources: EU EUDAMED, US FDA

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    SPACELINE FEEL 21

    FDA 510(k)
    FDA Class 1 ·Dental

    ITE HEARING AID, SOUND MED AMETHYST MODEL

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    PANTEX DIRECT TESTOSTERONE COATED TUBE RADIOIMMUNO

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    D901 LILLIPUT OXYGENATOR

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

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Injury ·INSULET CORPORATION·Product code LZG·February 1, 2013

    TORNIER

    FDA Adverse Event
    Malfunction ·TORNIER INC.·Product code KWS·December 2, 2010

    MONOPOLAR CURVED SCISSORS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·July 23, 2014

    CUSTOM PERFUSION PACK

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

    GMK-SPHERE PIN ADAPTOR HUDSON COUPLING - CONICAL ASSEMBLY

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code LXH·October 15, 2021

    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