BEUDAMED
    9 results · 20ms · 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 × Regulation: Us FDA × Clear all

    REBOUND HRD

    FDA Adverse Event
    Malfunction ·MINNESOTA MEDICAL DEVELOPMENT, INC.·Product code FTL·May 16, 2011

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 9, 2024

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 9, 2025

    CROSS PLATE MTP, RIGHT ANCHORAGE

    FDA Adverse Event
    Injury ·STRYKER GMBH·Product code HRS·November 27, 2024

    VA LOCKSCR 2.4 SELF-TAP L20 TAN

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWC·April 29, 2013

    GUGLIELMI DETACHABLE COIL (GDC)

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC - CORK·Product code HCG·May 10, 2011

    PROSTAR XL SUTURE-MEDIATED CLOSURE

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR REDWOOD CITY·Product code MGB·July 29, 2008

    CROSS PLATE MTP, RIGHT ANCHORAGE

    FDA Adverse Event
    Injury ·STRYKER GMBH·Product code HRS·November 25, 2024

    CROSS PLATE MTP, RIGHT ANCHORAGE

    FDA Adverse Event
    Injury ·STRYKER GMBH·Product code HRS·November 21, 2024