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

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    V-Laser

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

    ALARIS SMARTSITE

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS S.A DE C.V.·Product code FPA·January 26, 2026

    CLEARFIL SA PRIMER

    FDA 510(k)
    FDA Class 2 ·Dental

    UNIMED TEMPERATURE PROBE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SONICATH ULTRA 3.2

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP.·Product code ITX·October 30, 2008

    PROXIMATE** SKIN STAPLER 35 WIDE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDT·August 24, 2011

    NKII SINTERLOCK POROUS FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code JWH·July 5, 2013