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

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    Seclusion Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    InvisionECG System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NXSTAGE DIALYSATE PREPARATION MODULE, MODEL NX0269

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

    4.5MM CURVED BROAD LCP® PLATE 15 HOLES/282MM

    FDA Adverse Event
    Injury ·WRIGHTS LANE : SYNTHES USA PRODUCTS LLC·Product code HRS·January 19, 2018

    SERVO-S

    FDA Adverse Event
    Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·September 4, 2019

    CLARIUS ULTRASOUND SCANNER

    FDA Adverse Event
    Malfunction ·CLARIUS MOBILE HEALTH CORP.·Product code IYN·October 17, 2024

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·November 11, 2014

    IPUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 12, 2011

    PINNACLE MTL INS NEUT44IDX64OD

    FDA Adverse Event
    Injury ·8010379 DEPUY INTL., LTD.·Product code KWA·July 23, 2013