BEUDAMED
    7 results · 27ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    ULTRASOUND SYSTEMS DRAPE

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

    UNIVERSAL TAPER DELTA FEMORAL HEAD

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DD cubeX2 HS

    FDA 510(k)
    FDA Class 2 ·Dental

    PROULTRA ENDO TIPS

    FDA Adverse Event
    Malfunction ·DENTSPLY MAILLEFER·Product code ELC·June 8, 2006

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 21, 2013

    VISISTAT SKIN STAPLER 35W

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code GDT·January 4, 2011

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·July 31, 2014