BEUDAMED
    10 results · 28ms · Sources: EU EUDAMED, US FDA

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    STIMTECH TENS ELECTRODE

    FDA 510(k)
    FDA Class 2 ·Neurology

    Midwest Tradition® Pro

    FDA UDI
    SIRONA Dental Systems GmbH·E2767903450·Midwest Tradition® Pro TBF

    N.A.

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011790345000·topic Bracket with hook, - 22° Torque, 0° Angul...

    VPC

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MENDASIL TWG GEL ANTIMICROBIAL SKIN AND WOUND GEL

    FDA 510(k)
    FDA Unclassified ·Unknown

    TFNA HELICAL BLADE 95MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HSB·March 16, 2016

    ACCU-CHEK ® SPIRIT COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LZG·May 5, 2014

    EXTERNAL PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DTE·October 15, 2012

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·August 24, 2007

    ACCOLADE SR SL MRI (Model L310)

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025