BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    LITE TOUCH ERBIUM LASER TREATMENT SYSTEM

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

    Stainless Steel Tibial Nailing System

    FDA UDI
    ORTHOFIX SRL·18033509851049·TIBIAL NAIL LOCKING SCREW STERILE THREAD D 6 MM...

    SATC-1114, SHOULDER ABUTMENT TRANSFER COPING

    FDA 510(k)
    FDA Class 2 ·Dental

    MEDTRONIC MODEL 5407S, 5807S & 5410S SURG CABLES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code CBK·June 29, 2017

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·February 22, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 3, 2014

    COOK SPECTRUM

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FOZ·July 5, 2019