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

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    BOOMERANG WIRE /BOOMERANG PLUS WIRE SYSTEM, MODEL# B PLUS WIRE 58L

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Cordant

    FDA UDI
    Seaspine Orthopedics Corporation·10889981115425·85mm

    StrykeFlow

    FDA UDI
    STRYKER CORPORATION·07613327052046·Reusable Suction Irrigation Tip, Pool Suction, ...

    HYDRO2, HS-75

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    VENA TECH VENA CAVA FILTER; VENA TECH 30D VENA CAVA FILTER; VENA TECH LP CAVE FILTER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CELSITE ACCESS PORT

    FDA Adverse Event
    Malfunction ·B. BRAUN MEDICAL SAS·Product code LJT·October 23, 2014

    DEXTRUS 4135

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVN·April 22, 2013

    SM104 MSERIES W5TH WHL

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·March 29, 2011

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·July 7, 2008

    UNK

    FDA Adverse Event
    Injury ·VISTAKON·Product code LPL·October 11, 2010