BEUDAMED
    6 results · 21ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    M2A-MAGNUM PF CUP 54ODX48ID

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·April 27, 2026

    M2A-MAGNUM MOD HD SZ 48MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·April 27, 2026

    SITZ BATH 1616700692

    FDA Adverse Event
    Malfunction ·INVACARE CLEVELAND STREET·Product code KTC·July 22, 2015

    FLIXENE GW AND GWT GRAFTS > OR = 6MM

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORP.·Product code DSY·June 24, 2014

    ALCON ACCURUS 25+ GAUGE VITRECTOMY TOTAL PLUS PAK

    FDA Adverse Event
    Malfunction ·ALCON·Product code KYG·January 22, 2013

    EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDS·July 22, 2022