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

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    TERUMO ANGIOGTAPHIC CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    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

    VERTE-STACK® Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00721902379581·SPACER 8915414 14MM ADD ON LORDOTIC SM

    CVIS INSIGHT IMAGING CATHETERS

    FDA 510(k)
    FDA Class 2 ·Radiology

    MANGAR BOOSTER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    LOGIQ S7 DIAGNOSTIC ULTRASOUND SYSTEM

    FDA Adverse Event
    Malfunction ·GE ULTRASOUND KOREA CO., LTD.·Product code IYN·January 9, 2013

    AED PLUS

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·November 18, 2010

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC·Product code CBK·June 4, 2014