BEUDAMED
    11 results · 19ms · Sources: EU EUDAMED, US FDA

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    TRANSLUMINAL BALLOON DILATATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SYNERGY¿

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·November 4, 2015

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993305·anteriors; shade C1; mould BOM

    DynaClip Bone Staple

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ENHANCED ULTRA VIT PROBE

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·October 25, 2024

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·October 25, 2024

    AC-POWERED ADJUSTABLE HOSPITAL BED, INCLUDING RAILS

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code FNL·March 7, 2013

    TERUMO CDI 540 CALIBRATOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·December 23, 2010

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·August 8, 2014

    ENCOREANYWHERE

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·February 17, 2016