BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    MINI O2

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707057178·DB TUBE MIM CONV 22/18/51 OCC L

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707063186·TUBE MIM CONV 22/18/51 OCC LEFT

    Rampart-O

    FDA UDI
    SPINEOLOGY INC.·M7402812513·Rampart-O

    EBONY PTA 0.014 PERIPHERAL DILATATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LIQUICHEK LIPIDS CONTROL LEVEL 1, LIQUICHEK LIPIDS CONTROL LEVEL 2, MODELS 641 AND 642

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·December 29, 2022

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·December 5, 2022

    FUSION 8MM-60CM SUPP PERIPHERAL GRAFT

    FDA Adverse Event
    Injury ·MAQUET CARDIOVASCULAR, LLC·Product code DSY·May 5, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012

    PARADYM

    FDA Adverse Event
    Malfunction ·SORIN BIOMEDICA C.R.M., S.R.L.·Product code MRM·August 17, 2010