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

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    PRESSURIZER

    FDA 510(k)
    FDA Class 1 ·General Hospital

    LGN PS HIGH FLEX XLPE SZ 1-2 13MM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·August 9, 2017

    GII PS HI FLEX ISRT SZ 7-8 9

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·July 19, 2017

    Visible Patient Suite

    FDA 510(k)
    FDA Class 2 ·Radiology

    OXY-SERVE II OXYGEN CONSERVING REGULATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    LGN PS HIGH FLEX XLPE SZ 1-2 13MM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·August 9, 2017

    GII ARTICULAR INSERTER/EXTRACT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBH·February 9, 2018

    CAPSUREFIX

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·February 9, 2013

    VENTAK PRIZM 2

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 7, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 23, 2014