BEUDAMED
    1,085 results · 24ms · Sources: EU EUDAMED, US FDA

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    ARRHYTHMIA CENTRAL-OGP-7201

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    One Gloss PS Sample Pack

    FDA UDI
    SHOFU DENTAL CORPORATION·E235OGPSSAMPLE0·Contains DIs: E23501770; E23501760; E23501780

    OPTICAL GUIDANCE PLATFORM

    FDA Adverse Event
    Malfunction ·VARIAN MEDICAL SYSTEMS, INC.·Product code IYE·February 11, 2011

    OPTICAL GUIDANCE PLATFORM

    FDA Adverse Event
    Malfunction ·VARIAN MEDICAL SYSTEMS·Product code IYE·September 30, 2010

    ARTIS ZEE BIPLANE

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE, BUSINESS AREA ADVANCED THERAPY·Product code IZI·March 15, 2017

    ARTIS Q BIPLANE

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE GMBH·Product code OWB·December 18, 2019

    MULTITOM RAX

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE GMBH·Product code OWB·February 15, 2017

    ARTIS ONE

    FDA Adverse Event
    Injury ·SIEMENS SHENZHEN MAGNETIC RESONANCE LTD.·Product code OWB·July 22, 2019

    OPTICAL GUIDANCE PLATFORM

    FDA Adverse Event
    Malfunction ·VARIAN MEDICAL SYSTEMS·Product code IYE·October 13, 2010

    BD ULTRA FINE¿ PEN NEEDLE

    FDA Adverse Event
    Injury ·BD (SUZHOU)·Product code FMI·October 23, 2018

    YSIO

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE GMBH·Product code KPR·April 15, 2019

    AXIOM LUMINOS DRF

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE GMBH·Product code OWB·July 18, 2017

    ARTIS Q BIPLANE

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE GMBH- AT·Product code OWB·November 12, 2020

    OPTICAL GUIDANCE PLATFORM

    FDA Adverse Event
    Malfunction ·VARIAN MEDICAL SYSTEMS·Product code IYE·October 19, 2010

    BIO-MEDICUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code DWF·July 5, 2023

    BIO-MEDICUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code DWF·July 5, 2023

    MULTITOM RAX

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE GMBH·Product code OWB·August 11, 2021

    PERCEVAL SUTURELESS AORTIC HEART VALVE

    FDA Adverse Event
    Malfunction ·LIVANOVA CANADA CORP.·Product code LWR·January 11, 2017

    YSIO MAX

    FDA Adverse Event
    Malfunction ·SIEMENS AG·Product code KPR·February 11, 2015

    LUMINOS Lotus Max, Model 11574100 and Luminos dRF Max, Model 10762471

    FDA Recall
    Open, Classified ·Siemens Medical Solutions USA, Inc·Product code OWB·December 5, 2025