BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    CYTOQUANT HEP-2 CELLS, CATALOG #02-251

    FDA 510(k)
    FDA Class 1 ·Hematology

    KLEER(TM) ORTHODONTIC BRACKET

    FDA 510(k)
    FDA Class 1 ·Dental

    STORZ ULTRA-SOURCE HIGH OUTPUT ILLUMINATOR

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

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·January 22, 2013

    SPRINT QUATTRO SECURE S

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 14, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 10, 2014

    SWAN-GANZ CONTINUOUS CARDIAC CATHETER

    FDA Adverse Event
    Death ·EDWARDS LIFESCIENCES, PR·Product code KRA·November 11, 2011

    SWAN-GANZ CONTINUOUS CARDIAC CATHETER

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES, PR·Product code KRA·November 11, 2011

    SWAN-GANZ CONTINUOUS CARDIAC CATHETER

    FDA Adverse Event
    Death ·EDWARDS LIFESCIENCES, PR·Product code KRA·November 11, 2011

    SWAN-GANZ CONTINUOUS CARDIAC CATHETER

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES, PR·Product code KRA·November 11, 2011