BEUDAMED
    9 results · 23ms · Sources: EU EUDAMED, US FDA

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    NEXGEN COMPL. KNEE SOL. LEGACY POSTERIOR STABILIZED/CONSTRAINED CONDYLAR KNEE FEMORAL COMPONENTS/ARTICULAR SURFACES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TITANIUM NEXGEN LCCL FEMORAL SZ C-LT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 21, 2018

    NEXGEN LEGACY POSTERIOR STABILIZED ARTICULAR SURFACE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·June 16, 2016

    PACING/PSI KIT: 5 FR/6 FR 2-L

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code LDF·April 15, 2015

    ANYVIEW-500R Fluoroscopic Mobile X-Ray System

    FDA 510(k)
    FDA Class 2 ·Radiology

    CRYOCARE CS SURGICAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 24, 2014

    GREENLIGHT MOXY FIBER OPTIC

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS·Product code GEX·February 8, 2013

    INTERGARD HEPARIN KNITTED RADIALLY SUPPORTED

    FDA Adverse Event
    Other ·INTERVASCULAR·Product code DSY·January 7, 2011