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

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    BD VERITOR (TM) SYSTEM FOR RAPID DETECTION OF RSV

    FDA 510(k)
    FDA Class 1 ·Microbiology

    HHM

    FDA UDI
    Oticon A/S·05707131257697·H150, BTE 13 WL 100 DBL HHM

    Aileron Posterior Fusion System

    FDA UDI
    Life Spine, Inc.·00190837044183·Plate, Static Aileron, Canted 16mm

    Aileron Posterior Fusion System

    FDA UDI
    Life Spine, Inc.·00190837044176·Core, Static Aileron, Canted 16mm

    INTRAORAL BELSENSOR GOLD

    FDA 510(k)
    FDA Class 2 ·Dental

    PROWESS

    FDA 510(k)
    FDA Class 2 ·Radiology

    LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·August 8, 2016

    BOSTON SCIENTIFIC/ENCORE/ADVANTAGE

    FDA Adverse Event
    Malfunction ·BSC TULLAMORE·Product code MAV·October 30, 2009

    SENSOR ENLITE

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OZO·October 1, 2014

    POWER DRIVE

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code GEY·May 29, 2013

    PLATE CUTTER

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS SELZACH·Product code LXH·June 14, 2011

    UNKNOWN KNEE FEMORAL

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 18, 2019

    UNKNOWN KNEE TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 18, 2019

    UNKNOWN KNEE TIBIAL TRAY

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 18, 2019