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

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    CODMAN FLEXIBLE ENDOSCOPE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Combo Stimulator MT9000, Combo Stimulator LT7102, TENS Stimulator InTENSity 10

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    MINI TIGHTROPE FT REPAIR KIT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·September 4, 2020

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·June 5, 2019

    OXF ANATOMIC BRG RT LG SIZE 4

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·June 13, 2014

    ENDO GIA ROTICULATOR 30-2.5 SULU

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL·Product code GDW·October 8, 2010

    ABGII MODULAR SHORT NECK

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code MEH·December 6, 2012

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·November 23, 2017

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·June 4, 2018

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·October 7, 2019

    NEXUS AND NXT DETACHABLE COIL

    FDA Adverse Event
    Malfunction ·EV3 NEUROVASCULAR·Product code HCG·April 21, 2009

    NEXUS AND NXT DETACHABLE COIL

    FDA Adverse Event
    Malfunction ·EV3 NEUROVASCULAR·Product code HCG·April 21, 2009

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·May 10, 2024

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·September 27, 2019

    SPRYSTEP VECTOR, Custom made device dynamic ankle-foot orthosis (AFO) , Reference numbers: 17V1030, 17V2030, 17V1031, 17V2031, 17V1032, 17V2032, 17V1033, 17V2033, 17V1035, 17V2035, 17V1036, 17V2036, 17V1037, 17V2037

    FDA Enforcement
    Class II ·Completed·Townsend Design·January 17, 2024