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

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    MULTICROSS SUPPORT CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ArgenZ ST 98x18 ML A3

    FDA UDI
    ARGEN CORPORATION, THE·D818121763·Dental porcelain/ceramic restoration kit

    DIOPSYS NOVA VEP VISION TESTING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    RS2MI MUSCLE STIMULATOR FAMILY

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    BD VACUTAINER® SST¿ BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·May 8, 2018

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code LXH·February 10, 2020

    MAQUET HCU30 DEVICE

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DWC·October 5, 2016

    AMISTEM H FEMORAL STEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·May 8, 2013

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code ITJ·September 26, 2014

    IN-SITU PLATE CUTTER, UPPERFACE/MIDFACE

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS FREIBURG·Product code LXH·May 20, 2011