BEUDAMED
    6 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SPINNING SPIROS® CLOSED MALE LUER, PURPLE CAP

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FPA·June 12, 2019

    SPINNING SPIROS® CLOSED MALE LUER, PURPLE CAP

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FPA·June 5, 2019

    STEM: MINIMAX CEMENTLESS ANATOMICAL STEM RIGHT SIZE 6

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·October 1, 2020

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 28, 2014

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·January 9, 2013

    INFINITI VISION SYSTEM OZIL

    FDA Adverse Event
    Injury ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·November 19, 2010