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

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    Filters FDA Adverse Event ×

    K133532

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·February 2, 2021

    PHILIPS RESPIRONICS FACIAL CUSHION

    FDA Adverse Event
    Malfunction ·PHILIPS / RESPIRONICS, INC.·Product code BZD·April 8, 2026

    NELLCOR OXIMAX N-65

    FDA Adverse Event
    SANMINA-SCI SYSTEMS·Product code DQA·October 1, 2014

    MINICAP TRANSFER SET

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·May 29, 2013

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·June 15, 2011

    MATRIX LOCKING CAP WITHOUT SADDLE

    FDA Adverse Event
    Malfunction ·SYNTHES SELZACH·Product code NKB·February 16, 2015

    MATRIX LOCKING CAP WITHOUT SADDLE

    FDA Adverse Event
    Malfunction ·SYNTHES SELZACH·Product code NKB·February 16, 2015

    6.0MM TI MATRIX POLYAXIAL SCREW 40MM THREAD LENGTH

    FDA Adverse Event
    Malfunction ·SYNTHES SELZACH·Product code NKB·February 16, 2015