BEUDAMED
    8 results · 69ms · Sources: EU EUDAMED, US FDA

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    PVC AND SILICONE MANUAL RESUSCITATORS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NEOPUFF INFANT RESUSCITATOR

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTL·June 29, 2015

    NEOPUFF INFANT RESUSCITATOR

    FDA Adverse Event
    Malfunction ·Product code BTL·May 16, 2021

    HUDSON FOLDABLE MANUAL RESUS,DISP, ADULT W/FLO

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BTM·October 1, 2015

    NEOPUFF INFANT RESUSCITATOR

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTL·February 15, 2017

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Death ·ZOLL MANUFACTURING CORPORATION·Product code MVK·November 22, 2019

    EDWARDS SAPIEN 3 ULTRA RESILIA VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·January 30, 2026

    SHINEBALL PVC MANUAL RESUSCIATOR, ENT-1001, ENT-1003, ENT-1005, SHINEBALL SILICONE MANUAL RESUSCIATOR, ENT-1022,

    FDA 510(k)
    FDA Class 2 ·Anesthesiology