BEUDAMED
    10 results · 35ms · Sources: EU EUDAMED, US FDA

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    MOSS GASTROSTOMY TUBE

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

    VYGON SPLIT CANNULA INTRODUCER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ESTECH COBRA SURGICAL SYSTEM WITH THERMASHIELD ACCESSORY

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

    FLEXTEND

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·January 11, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Death ·CPI - DEL CARIBE·Product code NVY·November 30, 2010

    DELTAPAQ - CERECYTE MICROCOIL

    FDA Adverse Event
    Malfunction ·MICRUS ENDOVASCULAR, LLC·Product code HCG·July 2, 2014

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·February 13, 2026

    ECHELON ENDOPATH STAPLER

    FDA Adverse Event
    Injury ·Product code GDW·October 2, 2021

    FLEX 60 ARTICULATING

    FDA Adverse Event
    Injury ·Product code GDW·September 30, 2021

    Disposable Paper Filter for Sterilization Containers Paper, Medical Accessory, 100 DISP, Paper F, Steri.Cases, New Shape, Manufactured and distributed by Stryker Leibinger GmbH & Co KG, Distributed in the USA by: Stryker Orthopedics, NON STERILE.

    FDA Enforcement
    Class II ·Terminated·Stryker Craniomaxillofacial Division·October 14, 2015