BEUDAMED
    12 results · 23ms · Sources: EU EUDAMED, US FDA

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    DYNATRON 406 ELECTROTHERAPY APPARATUS

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111189357·JACKSON TUBE ORIG SHORT #8 STL

    ONIS-PACS

    FDA 510(k)
    FDA Class 2 ·Radiology

    ONETOUCH ZOOM DIABETES MANAGEMENT PROGRAM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    KIT IMPLANTABLE SLIM TIP LEAD, 50CM

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code PMP·September 29, 2023

    KIT IMPLANTABLE SLIM TIP LEAD, 50CM

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code PMP·September 29, 2023

    KIT IMPLANTABLE SLIM TIP LEAD, 50CM

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code PMP·March 12, 2026

    KIT IMPLANTABLE SLIM TIP LEAD, 50CM

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code PMP·March 12, 2026

    KIT IMPLANTABLE SLIM TIP LEAD, 50CM

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code PMP·March 12, 2026

    RESTORATION ADM X3 INS

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LZO·April 30, 2014

    ARTICULEZE M HEAD 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code JDI·October 10, 2012

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·July 28, 2010