BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    MODIFIED TREVO PROVUE RETRIEVER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Oticon

    FDA UDI
    Oticon A/S·05707131261311·H11, BTE 13 WL 85 CNB

    PACIFIC XTREME PTCA BALLOON DILATATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EDWARDS LIFESCIENCES RESEARCH MEDICAL PEDIATRIC VENOUS RETURN CANNULAE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD PLASTIPAK SYRINGE

    FDA Adverse Event
    Injury ·BD·Product code FMF·September 26, 2012

    7MM TI STRAIGHT RADIAL STEM 26MM-STERILE

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code KWI·February 2, 2015

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·May 29, 2013

    INNOVA 2121 - IQ

    FDA Adverse Event
    Injury ·GE MEDICAL SYSTEMS S.C.S.·Product code MQB·June 15, 2011

    RESOLUTION CLIP DEVICE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MND·August 22, 2008