BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    ANGIOCATH(R) NONVALON(R) AND ANGIO-SET(R) IV CATHETERS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BD ANGIOCATH¿ IV CATHETER 22 G X 1"

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·September 13, 2017

    BD ANGIOCATH¿ IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FOZ·August 8, 2017

    BASE

    FDA UDI
    Nuvasive, Inc.·00887517700391·BASE Guide, A

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04064984699533·GENUMEDI PSS BLUE, SIZE I

    SpiritMB

    FDA UDI
    ORMCO CORPORATION·00889989007374·ID K - Twin - Upper-Left Cuspid - Green

    MRIDIUM 3850 MRI PUMP SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NavSuite3 Kit

    FDA 510(k)
    FDA Class 2 ·Neurology

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·February 8, 2013

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·December 14, 2010

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·July 22, 2014