BEUDAMED
    8 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.35 WIRE, 12, STERILE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·August 11, 2021

    BD ALARIS¿ SMARTSITE¿ GRAVITY SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·February 9, 2023

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILLROM DE MEXICO S DE RL DE CV·Product code FPO·April 15, 2014

    UNKNOWN_RECONSTRUCTIVE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·January 28, 2013

    GEMSTAR PAIN MGE SNG

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code FRN·November 22, 2010

    BD GEM V/NV 20D 0.2 FLTR

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·July 28, 2022

    GEM V/NV NTG 20DP 20PK

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·November 10, 2020

    BD ALARIS¿ SMARTSITE¿ GRAVITY SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·January 20, 2023