BEUDAMED
    9 results · 24ms · Sources: EU EUDAMED, US FDA

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    SLENDERTONE CoreFit Abs 8, Type 734

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    MYLABGOLD

    FDA 510(k)
    FDA Class 2 ·Radiology

    C-QUR LITE MESH V-PATCH

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

    TRANSCEND 365 MINICPAP SYSTEM

    FDA Adverse Event
    Injury ·SOMNETICS INTERNATIONAL, INC.·Product code BZD·October 6, 2021

    BD ANGIOCATH IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·May 13, 2020

    UNK GEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·UNKNOWN MANUFACTURER·Product code FTR·February 27, 2018

    11CM ANGLE ATTACHMENT, BLACK MAX

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBE·October 17, 2014

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 20, 2013

    VASOVIEW HEMOPRO EVH SYSTEM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·July 7, 2011