BEUDAMED
    10 results · 31ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    INSPIRE 8F DUAL HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER AND HARDSHELL RESERVOIR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    INSPIRE HVR DUAL

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA·Product code DTN·November 12, 2024

    INSPIRE HVR DUAL HARDSHELL VENOUS/CARDIOTOMY RESERVOIR

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA SRL·Product code DTZ·November 18, 2022

    ArgenZ HT+ 98x18 A2

    FDA UDI
    ARGEN CORPORATION, THE·D818122844·Dental porcelain/ceramic restoration kit

    ALL-BOUND 3

    FDA 510(k)
    FDA Class 2 ·Dental

    SYNTHES RESORBABLE CONTOURABLE MESH

    FDA 510(k)
    FDA Class 2 ·Dental

    AMPLATZ SUPER STIFF GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA (HEREDIA)·Product code DQX·May 21, 2013

    FREESTYLE FREEDOM LITE

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC,·Product code NBW·January 14, 2011

    UNKNOWN DEPUY ASR HIP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 3, 2011

    MANTIS REDUX BLOCKER

    FDA Adverse Event
    Malfunction ·STRYKER SPINE-US·Product code NKB·November 27, 2019