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

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    VERTEX PERCUTANEOUS CATHETER INTRODUC

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ABC CAUDAL AND CRANIAL EXTENSION PLATE (E-PLATE)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TRANSONIC HCM 102 SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UNKNOWN ASR UNI FEMORAL HEAD

    FDA Adverse Event
    Injury ·Product code KWA·November 20, 2012

    ASR ACETABULAR CUPS 52

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD - 8010379·Product code KWA·May 30, 2014

    ACCU-CHEK ® COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·September 21, 2010

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·November 23, 2017