BEUDAMED
    33 results · 24ms · Sources: EU EUDAMED, US FDA

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    PlasmaWave

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    COMPREHENSIVE SRS

    FDA UDI
    Biomet Orthopedics, LLC·00880304540767·

    Comprehensive® SRS / Discovery®

    FDA UDI
    Biomet Orthopedics, LLC·00880304850330·

    ARTHREX DISTAL EXTREMITY PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FLAVORED MALE LATEX CONDOM

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

    ADVANTAGE FIT ULTRA SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OTN·November 7, 2025

    ADVANTAGE FIT ULTRA SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OTN·January 9, 2026

    ADVANTAGE FIT ULTRA SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OTN·January 9, 2026

    ADVANTAGE FIT ULTRA SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OTN·May 23, 2025

    ADVANTAGE FIT ULTRA SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OTN·March 25, 2026

    ADVANTAGE FIT ULTRA SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OTN·October 28, 2025

    LYNX ULTRA SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OTN·December 12, 2025

    LYNX ULTRA SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OTN·September 4, 2025

    UNKKNOWN PROXIMAL BODY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDC·March 1, 2018

    COMPREHENSIVE SRS MOD STEM - 10X100MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDC·March 1, 2018

    COMPREHENSIVE SRS IC SEG - 30MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDC·March 1, 2018

    UNKNOWN REGENERX AUGMENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDB·March 1, 2018

    GEMSTAR 7 THERAPY PUMP

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code FRN·October 16, 2008

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE - ANDOVER·Product code MKJ·July 11, 2011

    CONTAK RENEWAL

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 8, 2013