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

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    FLEX-AID LIQUID GEL BANDAGE AND DERMAFLEX GEL TISSUE ADHESIVE PROFESSIONAL LIQUID BANDAGE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Ipsoclip

    FDA UDI
    Cendres+Métaux SA·07640173092209·Ipsoclip anterior, Bayonett lock O

    LFIT V40 FEMORAL HEAD COMPONENTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VARELISA CARDIOLIPIN IGA ANTIBODIES, MODELS 15748 & 15796

    FDA 510(k)
    FDA Class 2 ·Immunology

    9611993-2022-050757

    FDA Adverse Event
    Injury ·NOBEL BIOCARE (PRODUCTION) AB·Product code DZE·March 28, 2022

    BD PHOENIX¿ SMIC-101

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 13, 2026

    ARCOS 18X150MM SPL TPR DIST HA

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·December 7, 2016

    ARCOS HA MODULAR REVISION SYSTEM CONE PROXIMAL BODY 60MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·December 7, 2016

    ARCOS HA MODULAR REVISION SYSTEM STRAIGHT TAPERED SPLINED DISTAL STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·January 10, 2017

    ARCOS HA MODULAR REVISION SYSTEM CONE PROXIMAL BODY / TYPE 1 TAPER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·January 10, 2017

    BIPAP AUTO M-SERIES

    FDA Adverse Event
    Death ·RESPIRONICS, INC·Product code BZD·July 11, 2012

    BIPAP AUTO SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 9, 2022

    BIPAP AUTO SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 14, 2022

    BIPAP AUTO BIFLEX

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 14, 2022

    HOLDING SLEEVE-LONG FOR MATRIX

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code LXH·April 10, 2013

    PUMP IN STYLE ADVANCE METRO BAG

    FDA Adverse Event
    Injury ·MEDELA, INC.·Product code HGX·March 31, 2011

    RIATA ST OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 27, 2008

    ARCOS DISTAL SCREW TI DIA5X50MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·October 12, 2016

    ARCOS DISTAL SCREW TI DIA5X45MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·October 12, 2016

    BIPAP AUTO SERIES ASSY

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 31, 2022