BEUDAMED
    6 results · 34ms · Sources: EU EUDAMED, US FDA

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    DRESSING CHANGE TRAY

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PROCOLL

    FDA 510(k)
    FDA Unclassified ·Unknown

    DORNIER DIODE LASER FAMILY MEDILAS D, MEDILAS D SKINPULSE & MEDILAS D SKINPULSE S LASER SYSTEM

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

    ASR 300 SPIKED CUP SIZE 50

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 17, 2013

    JOSTENT GRAFTMASTER

    FDA Adverse Event
    Death ·AV-RANGENDINGEN·Product code MAF·December 10, 2010

    PROGRASP FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·July 8, 2014