BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Quickdent Dental Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    EASYSPINE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    QuantaFlo

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MPACT 3D METAL

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·May 8, 2026

    PARIETENE PROGRIP RT PPL/PLA 12X8CM

    FDA Adverse Event
    Malfunction ·TREVOUX - USS·Product code FTL·November 21, 2008

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·September 11, 2011

    RUSCH 100% SILICONE FOLEY 6 FR

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code KOD·July 18, 2013

    PEN NEEDLE 31GX5MM 14 PACK

    FDA Adverse Event
    Malfunction ·EMBECTA MEDICAL DEVICES (SUZHOU) CO., LTD., CHINA·Product code FMI·May 19, 2025

    Model Number L111, ESSENTIO DR SL MRI Pacemaker

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