BEUDAMED
    14 results · 22ms · Sources: EU EUDAMED, US FDA

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    ELLAGIC ACID APTT REAGENT

    FDA 510(k)
    FDA Class 2 ·Hematology

    VERTE-STACK® Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00721902379604·SPACER 8915418 18MM ADD ON LORDOTIC SM

    GATES GLIDDEN DRILLS

    FDA 510(k)
    FDA Class 1 ·Dental

    LIFE-TRACE DISPOSABLE LEG PLATE PRODUCT # LT-100

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    HEARTMATE II LVAS, EUROPE

    FDA Adverse Event
    Malfunction ·THORATEC CORP.·Product code DSQ·June 5, 2014

    TERUMO CDI 500 BLOOD PARAMETER MONITOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·January 9, 2013

    DUAL CUT SAGITTAL BLADE

    FDA Adverse Event
    Malfunction ·STRYKER IRELAND LTD.·Product code HWE·November 4, 2010

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·July 14, 2020

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·July 3, 2024

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·Product code DQO·November 3, 2020

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·Product code DQO·November 3, 2020

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·Product code DQO·November 3, 2020

    RADIFOCUS GLIDECATH

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·January 24, 2023

    RADIFOCUS ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQO·September 26, 2018