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

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    CENTRIX'S ENCORE NATURAL COMPOSITE RESIN CORE PAST

    FDA 510(k)
    FDA Class 2 ·Dental

    SCORPIO LOW PROFILE TIBIAL TRAY

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    QUADROX-I, QUADROX-ID, QUADROX-IR OXYGENATORS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC·Product code KWP·December 18, 2014

    AED PRO

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·December 1, 2010

    ACCURUS 800CS

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·March 11, 2014

    PRIME ZOOM STRETCHER, ELECTRIC

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code INK·December 28, 2012

    HLM TUBING SET W/SOFTLINE COATING

    FDA Adverse Event
    Injury ·MAQUET CARDIOPULMONARY AG·Product code DTZ·November 18, 2015

    HLM TUBING SET W/SOFTLINE COATING

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·June 3, 2016

    HLM TUBING SET W/BIOLINE COATING

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·August 2, 2016