BEUDAMED
    13 results · 25ms · Sources: EU EUDAMED, US FDA

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    ThinkMed Intermittent Catheter with/without Hydrophilic Coating

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

    DATAPRO CLINICAL CHELISTRY ANALYZER

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CARDIO XP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LSLF EXT SET W CLV

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code FPA·May 24, 2013

    CARPENTIER-EDWARDS PHYSIO ANNULOPLASTY RING

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code KRH·August 27, 2008

    MBT CEM KEEL TIB TRAY SZ5

    FDA Adverse Event
    Injury ·DEPUY-CORK, A DIVISION OF DEPUY ORTHOPAEDICS·Product code NJL·June 23, 2011

    DISCARDIT¿ II SYRINGE W/O NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·December 26, 2018

    BD DISCARDIT II SYRINGE W/O NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·February 5, 2019

    BD DISCARDIT¿ II SYRINGE W/O NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·December 19, 2018

    BD DISCARDIT¿ II SYRINGE W/O NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·December 27, 2018

    BD AffirM VPIII Microbial Identification Test

    FDA Enforcement
    Class II ·Terminated·Becton Dickinson & Co.·March 8, 2017

    DISCARDIT II SYRINGE W/O NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 2, 2019

    BD DISCARDIT II SYRINGE W/O NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·February 6, 2019