BEUDAMED
    21 results · 23ms · Sources: EU EUDAMED, US FDA

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    NeuroBlate Fusion-S Software V3.17

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    GII QUICKANCHOR ORTHOCORD

    FDA UDI
    Medos International Sàrl·10886705008612·GII QUICKANCHOR Plus Size 2 (5 metric) ORTHOCOR...

    GII QA+ O/C CP-2 *EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code JDR·December 6, 2018

    BARDPORT X-PORT ISP PORT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    KSEA BIPOLAR ELECTRODE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    GII QA+ W #2 ORTHOCORD

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code JDR·September 18, 2014

    MAXZERO NEEDLELESS CONNECTOR

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FPA·March 1, 2017

    TENDRIL SDX

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·November 10, 2008

    LSLF EXT SET W CLV

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code FPK·August 10, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·July 12, 2013

    GII QA+ O/C CP-2 *EA

    FDA Adverse Event
    Injury ·DEPUY MITEK LLC US·Product code JDR·April 16, 2019

    GII QA+ O/C CP-2 *EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code JDR·January 29, 2019

    GII QA+ O/C CP-2 *EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code JDR·January 29, 2019

    GII QA+ O/C CP-2 *EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code JDR·October 16, 2018

    GII QA+ W #2 ORTHOCORD

    FDA Adverse Event
    Injury ·DEPUY MITEK LLC US·Product code JDR·April 17, 2019

    RC LOOP (DB) ANCHOR W/ORTHOCORD GII QA+ W #2 ORTHOCORD

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code JDR·July 5, 2022

    RC LOOP (DB) ANCHOR W/ORTHOCORD GII QA+ W #2 ORTHOCORD

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code JDR·July 6, 2022

    GII QA+ O/C CP-2 *EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code JDR·March 19, 2018

    SUPER QUICKANCHOR+ DS W/#2 ORTHOCORD

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code JDR·September 26, 2017

    SUPER QUICKANCHOR+ DS W/#2 ORTHOCORD

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code JDR·September 26, 2017