BEUDAMED
    12 results · 30ms · Sources: EU EUDAMED, US FDA

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    STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTS

    FDA 510(k)
    FDA Class 1 ·Cardiovascular

    SmartBand EMR Kit, SmartBand EMR Pack, SmartSnare

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

    POWERPORT DUO M.R.I. IMPLANTED PORT WITH 9.5 FR. DUAL LUMEN CHRONOFLEX POLYURETHANE CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·March 5, 2013

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·August 8, 2014

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·February 15, 2011

    BD BACTEC¿ MYCO/F LYTIC CULTURE VIALS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·March 20, 2023

    BD BACTEC¿ MYCO/F LYTIC CULTURE VIALS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·November 4, 2025

    BD BACTEC¿ MYCO/F LYTIC CULTURE VIALS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·January 11, 2023

    BD BACTEC¿ MYCO/F LYTIC CULTURE VIALS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·September 9, 2022

    BD BACTEC¿ MYCO/F LYTIC CULTURE VIALS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·July 8, 2022

    BD BACTEC¿ MYCO/F LYTIC CULTURE VIALS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·February 1, 2022