BEUDAMED
    12 results · 18ms · Sources: EU EUDAMED, US FDA

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    ANGIOCATH & INSYTE AUTOGUARD CATHETERS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    INSYTE AUTOGUARD PNK 20GA X 1.16IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 14, 2019

    BD INSYTE AUTOGUARD SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 18, 2020

    BD INSYTE AUTOGUARD SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 18, 2020

    BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·December 27, 2018

    INSYTE-N AUTOGUARD YEL 24GA X .56IN

    FDA Adverse Event
    Malfunction ·Product code FOZ·September 14, 2021

    BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·May 23, 2019

    MODIFICATION TO:SANARUS VISICA TREATMENT SYSTEM , MODELS VS2000

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

    Aquasil Ultra + Smart Wetting Impression Material

    FDA 510(k)
    FDA Class 2 ·Dental

    CARELINK

    FDA Adverse Event
    Injury ·RICE CREEK MFG·Product code KRG·February 9, 2013

    DC BEAD

    FDA Adverse Event
    Death ·BIOCOMPATIBLES UK LTD·Product code HCG·July 17, 2014

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·January 7, 2011