BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    KENDALL SCDS

    FDA Adverse Event
    Injury ·KENDALL MC RAW·Product code JOW·January 6, 2004

    6308 2000 ML DRAIN BG W/SPOUT

    FDA Adverse Event
    Injury ·CARDINAL HEALTH·Product code KNX·August 8, 2023

    PREFORM GUIDEWIRE - SAFARI2

    FDA Adverse Event
    Injury ·LAKE REGION MEDICAL·Product code DQX·June 8, 2016

    LIPPES LOOP DOUBLE S INTRAUTERINE DEVICE

    FDA Adverse Event
    Injury ·R.W. JOHNSON PHARM. RESEARCH INSTITUTE DIV OF ORTHO PHARMACEUTICAL CORP.·Product code HDT·September 11, 1997

    LIPPES LOOP DOUBLE S INTRAUTERINE DEVICE

    FDA Adverse Event
    Injury ·R.W. JOHNSON PHARM. RESEARCH INSTITUTE DIV. OF ORTHO PHARMACEUTICAL CORP·Product code HDT·August 11, 1998

    LIPPES LOOP DOUBLE S INTRAUTERINE DEVICE

    FDA Adverse Event
    Injury ·R.W. JOHNSON PHARM. RESEARCH INSTITUTE/DIV. OF ORTHO PHARMACEUTICAL CORP·Product code HDT·June 10, 1998

    ALL-FLEX ARCING SPRING DIAPHRAGM

    FDA Adverse Event
    Injury ·R.W. JOHNSON PHARM. RESEARCH INSTITUTE/DIV OF ORTHO PHARMACEUTICAL CORP.·Product code HDW·June 10, 1998