BEUDAMED
    10 results · 36ms · Sources: EU EUDAMED, US FDA

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    MOVIT DEVICE

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    Bosworth Rimseal

    FDA UDI
    Harry J Bosworth Company·H66809217101·Rimseal PEMA Impression Material P&L Kit

    XPERT CT/NG

    FDA 510(k)
    FDA Class 2 ·Microbiology

    NAGASHIMA NX-150F LIGHT SOURCE UNIT

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

    DHS®/DCS® LAG SCREW 12.7MM THREAD/100MM-STERILE

    FDA Adverse Event
    Malfunction ·SYNTHES·Product code KTT·January 18, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code FRN·February 6, 2014

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 13, 2010

    BI-METRIC/X POR NC LAT 16X160

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·July 25, 2019

    M2A-MAGNUM MOD HD SZ 50MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·January 17, 2019

    M2A-MAGNUM PF CUP 56ODX50ID

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·January 17, 2019