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

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    ASAHI GUIDE WIRE EXTENSION 165CM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Disposable Blade

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113202·BARD-PARKER BLADE #15 PACK OF 50

    INTRODEUCE DOUBLE LUMEN INTRODUCER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SMITH & NEPHEW PHOENIX 5.0 ALLOGRAFT ANCHOR KIT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·Product code MNT·March 29, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·Product code MNT·May 27, 2021

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 6, 2013

    6800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 18, 2011

    BIPOLAR LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·August 6, 2008

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code MNT·May 6, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·Product code MNT·March 24, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·Product code MNT·June 15, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·Product code MNT·May 18, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·Product code MNT·June 7, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·Product code MNT·April 2, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·Product code MNT·April 8, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·Product code MNT·April 16, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·Product code MNT·April 28, 2021

    V60 VENTILATOR

    FDA Adverse Event
    Malfunction ·Product code MNT·November 24, 2020

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·Product code MNT·July 2, 2021