BEUDAMED
    10 results · 26ms · Sources: EU EUDAMED, US FDA

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    DESERET(R) I.V. LOOP AND DESERET (R) J LOOP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04064984699557·GENUMEDI PSS BLUE SIZE III

    BASE

    FDA UDI
    Nuvasive, Inc.·00887517700414·BASE Guide, C

    XXL Vascular Balloon Dilatation Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    5 SEC DIGITAL CLINICAL THERMOMETER, MODELS ST8630X, ST8640X, ST8730X, ST8740X, ST8930X, ST8940X, ST8030X, ST8040X.

    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

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·February 8, 2013

    SWEET PICOTIP

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·January 6, 2011

    ENDURANT II

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·July 22, 2014

    BD ANGIOCATH¿ IV CATHETER

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