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

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    ACS VIKING GUIDING CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    A-CIFT SoloFuse

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CYNOSURE YAG FAMILY LASER

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CERTAIN¿ TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code NHA·July 27, 2023

    STERRAD 200 STERILIZER

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·February 21, 2013

    ASPHERE M SPEC 12/14 36 +5

    FDA Adverse Event
    Injury ·DEPUY INTL LTD.·Product code KWA·January 26, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·August 1, 2014

    CERTAIN¿ TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code NHA·July 27, 2023