BEUDAMED
    10 results · 25ms · Sources: EU EUDAMED, US FDA

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    MixJect® Transfer Device

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Men's Liberty

    FDA UDI
    ARGENTUM MEDICAL, LLC·00653599001790·Men's Liberty for iMEDicare, (pack of 4)

    CARESTREAM DRX-1 SYSTEM WITH DRX 2530C DETECTOR

    FDA 510(k)
    FDA Class 2 ·Radiology

    GEM, MODEL 004110

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BD PEGASUS GN 18GA X 1.16IN PRN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL DEVICES CO., LTD. SUZHOU·Product code FOZ·April 8, 2022

    LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·November 7, 2008

    ASR UNI FEMORAL IMPL SIZE 55

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·September 1, 2011

    LYNX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·July 16, 2013

    MAZOR X SYSTEM

    FDA Adverse Event
    Malfunction ·MAZOR ROBOTICS LTD·Product code OLO·January 1, 2026

    CODMAN Disposable Perforator, 14mm. Cranial perforator.

    FDA Enforcement
    Class I ·Ongoing·Integra LifeSciences Corp. (NeuroSciences)·May 14, 2025