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

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    PRISMAFLEX

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PRISMAFLEX

    FDA Adverse Event
    Injury ·GAMBRO LUNDIA AB·Product code KDI·February 6, 2014

    PRISMAFLEX

    FDA Adverse Event
    Death ·GAMBRO LUNDIA AB·Product code KDI·April 11, 2014

    PRISMAFLEX

    FDA Adverse Event
    Injury ·GAMBRO LUNDIA AB·Product code KDI·November 2, 2012

    PRISMAFLEX

    FDA Adverse Event
    Injury ·GAMBRO LUNDIA AB·Product code KDI·February 15, 2012

    PRISMAFLEX

    FDA Adverse Event
    Injury ·GAMBRO LUNDIA AB·Product code KDI·December 23, 2013

    PRISMAFLEX

    FDA Adverse Event
    Injury ·GAMBRO LUNDIA AB·Product code KDI·February 6, 2014

    PRISMAFLEX

    FDA Adverse Event
    Death ·GAMBRO LUNDIA AB·Product code KDI·January 10, 2014

    PRISMAFLEX

    FDA Adverse Event
    Death ·GAMBRO LUNDIA AB·Product code KDI·January 3, 2014

    PRISMAFLEX

    FDA Adverse Event
    GAMBRO LUNDIA AB·Product code KDI·February 6, 2014

    PRISMAFLEX

    FDA Adverse Event
    Injury ·GAMBRO LUNDIA AB·Product code KDI·August 13, 2012

    PRISMAFLEX

    FDA Adverse Event
    Injury ·GAMBRO LUNDIA AB·Product code KDI·January 10, 2014

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306818738·Malleable Retractor 6" x 12" w/ Protective Edge

    DONJOY

    FDA UDI
    DJO, LLC·00888912152556·DRESSING,UNIVERSAL,XL, STERILE

    WOUND PRO APEX

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

    SPAZZ

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    VENTED AUTOFEED CHAMBER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·April 23, 2012

    HYDRATOME? RX 44

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA (COYOL)·Product code KNS·May 14, 2013

    UNICEL® DXC 600 PRO SYNCHRON® CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·June 1, 2011

    STERI-CATH CLOSED VENTILATION SYSTEM

    FDA Adverse Event
    Injury ·SMITHS HEALTHCARE MANUFACTURING S.A. DE C.V.·Product code BSY·August 4, 2008