BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    MICROSURGICAL KNIVES, 20, 30, 45

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    SpaceOAR System

    FDA 510(k)
    FDA Class 2 ·Radiology

    AXIUM DETACHABLE COIL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TRUEMETRIX

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH, INC.·Product code NBW·September 19, 2016

    SIZE 3 ACCOLADE II 127 DEG

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·April 30, 2014

    PROMOTE PLUS CRT-D, DF-4 CONNECTOR

    FDA Adverse Event
    Death ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·October 10, 2012

    COLLEAGUE CXE VOLUMETRICINFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 3, 2010

    AXIUM

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 10, 2019

    AXIUM

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 10, 2019

    AXIUM

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 10, 2019

    AXIUM

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 11, 2019