BEUDAMED
    8,005 results · 68ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    THORAGUARD SYSTEM

    FDA Adverse Event
    Malfunction ·CENTESE, INC·Product code BTA·August 9, 2025

    THOROGUARD

    FDA Adverse Event
    Injury ·CENTESE, INC.·Product code BTA·June 24, 2025

    ALABAMA TISSUE CENTER, INC.

    FDA Adverse Event
    Other ·UNK·Product code MIE·October 7, 2004

    CUSTOM ULTRASONICS INC. SYSTEM 83 PLUS

    FDA Adverse Event
    Malfunction ·CUSTOM ULTRASONICS INC·Product code KOG·December 21, 2012

    ULTHERA SYSTEM

    FDA Adverse Event
    Injury ·ULTHERA, INC., MERZ DEVICE INNOVATION CENTER·Product code OHV·October 3, 2017

    ULTHERA SYSTEM

    FDA Adverse Event
    Injury ·ULTHERA, INC., MERZ DEVICE INNOVATION CENTER·Product code OHV·October 3, 2017

    PULMONETIC

    FDA Adverse Event
    Malfunction ·PULMONETIC SYSTEMS, INC.·Product code CBK·September 12, 2002

    WHITESTAR SIGNATURE SYSTEM

    FDA Adverse Event
    Malfunction ·JOHNSON & JOHNSON SURGICAL VISION, INC·Product code HQC·October 23, 2018

    ADVIA 2120I WITH DUAL ASPIRATE AUTOSAMPLER

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code GKZ·July 15, 2016

    INTRALASE FS2

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code HNO·March 14, 2018

    INTRALASE FS2

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC·Product code HNO·March 15, 2018

    INTRALASE FS2

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code HNO·March 28, 2018

    INTRALASE FS2

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC·Product code HNO·March 26, 2018

    INTRALASE FS2

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC·Product code HNO·April 3, 2018

    COLONOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDF·May 21, 2026

    EC-5000CXIII

    FDA Adverse Event
    Malfunction ·NIDEK INCORPORATED·Product code HQF·November 7, 2016

    VASSCAN TABLE MODEL 2184

    FDA Adverse Event
    Other ·MEDICAL POSITIONING, INC.·Product code LGX·September 1, 2009

    SELOX ST 60

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code DTB·December 4, 2009

    8.5F DIREX STEERABLE SHEATH

    FDA Adverse Event
    Injury ·OSCOR INC.·Product code DYB·May 7, 2019

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·October 11, 2022