BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

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    ROCKET ELECTRODE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150751·K-WIRE - SINGLE TROCAR 1.25mm DIA x 200mm

    ACCUCOM 2

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SMART SCALE X-RAY PLATFORM

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PROFILE BIABUT 4.0 -Ø5.5

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·February 24, 2026

    PCA3 MEDNET WIRELESS

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code MEA·February 19, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

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

    IRC2100 W/ 210 LIGHTGUIDE

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code KNS·August 28, 2019