BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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

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

    ARROW BIPOLAR PACING/BALLOON WEDGE PRESSURE CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MODIFICATION TO BODYGUARD INFUSION PUMP SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PointerShell Universal, PointerShell LS

    FDA 510(k)
    FDA Class 2 ·Neurology

    TITANIUM NEXGEN LCCL FEMORAL SZ C-LT

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

    2520274-2013-10220

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code MNI·February 11, 2013

    UNICEL® CLOSED TUBE ALIQUOTTER (UCTA) UNIT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·January 13, 2011

    DUROM ACETABULAR COMPONENT 58/52 CODE R

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·July 15, 2014

    NEXGEN LEGACY POSTERIOR STABILIZED ARTICULAR SURFACE

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