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

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    OSTEONICS OMNIFIT-C CEMENTED HIP STEM (LINE EXTENSION)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PRESTIGE® LP Cervical Disc System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994493705·PRESTIGE LP DISC 6X14MM

    ETHIPARAT Sterile

    Device
    EU MDR · Eu Md Class 1 ·Ansell Healthcare Europe NV·On the market·32 countries

    ADHEAR System

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    HI-TORQUE BALANCE MIDDLEWEIGHT UNIVERSAL II GUIDE WIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    840 VENTILATOR

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

    BVI 3000 DOME PROBE ASSY

    FDA Adverse Event
    Malfunction ·VERATHON INCORPORATED·Product code IYO·February 15, 2013

    POWER PRO AMBULANCE COT

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIV.·Product code INK·December 30, 2010

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 1, 2014

    PECTUS SYSTEM JANTON 12" TI PECTUS BAR 3.048CM (12") (L) TITANIUM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HRS·January 2, 2019