BEUDAMED
    6 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    6000008-1997-00030

    FDA Adverse Event
    Malfunction ·Product code GCY·February 13, 1997

    AP402-01 HCR - MICROBORE YELLOW MARKED WITH NON-VENTED SPIKE

    FDA Adverse Event
    Malfunction ·Q CORE MEDICAL LTD.·Product code FPA·March 22, 2016

    PORTEX 8.0MM SUCTIONAID TRACHEOSTOMY TUBE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL INTL, LTD.·Product code JOH·February 17, 2011

    POWERLED TM

    FDA Adverse Event
    Malfunction ·MAQUET SAS·Product code FSY·January 12, 2026

    PULSAR 2 GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY·Product code GEI·March 15, 2016

    OASIS

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code KDQ·January 26, 2025