BEUDAMED
    9 results · 27ms · Sources: EU EUDAMED, US FDA

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    NASO-LARYNGO-PHARYNGOSCOPE

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    MaXcess

    FDA UDI
    Nuvasive, Inc.·00887517200280·MaXcess-C Blade, 60mm Medial

    GOAT ANTI-HUMAN C-REACTIVE PROTEIN

    FDA 510(k)
    FDA Class 2 ·Immunology

    Turnpike Catheter; Turnpike Spiral Catheter; Turnpike Gold Catheter; Turnpike LP Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LIGACLIP** ENDOSCOPIC CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·March 6, 2013

    VERSA DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code NVZ·February 15, 2011

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MPRI·Product code NVY·August 8, 2014

    M2A-MAGNUM PF CUP 48ODX42ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 20, 2016

    M2A-MAGNUM MOD HD SZ 42MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 20, 2016