BEUDAMED
    64 results · 23ms · Sources: EU EUDAMED, US FDA

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    TELERADPRO

    FDA 510(k)
    FDA Class 2 ·Radiology

    N/A

    FDA UDI
    GEORGE TIEMANN & CO.·B5821024760·

    Blade Scalpel

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113530·SLIT BLADE 3.0MM ANGLED (BX/5)

    MONARCH, TRANSSHAPING GASTROSTOMY TUBE MODEL 9-2010

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

    LUMBOPERITONEAL SHUNT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·April 17, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·October 7, 2020

    LIGASURE

    FDA Adverse Event
    Injury ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·July 21, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·February 20, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·November 26, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·June 9, 2021

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·February 2, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·November 13, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·April 16, 2019

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·April 24, 2020

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·March 14, 2019

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·June 16, 2021

    GLOBAL UNITE HEAD 40X18 ECC

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code KWS·May 9, 2013

    TERUMO CDI 500 BLOOD PARAMETER MONITOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·May 20, 2011

    PULSE GEN MODEL

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·August 8, 2008