BEUDAMED
    18 results · 19ms · 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 Status: Injury ×

    6000023-2013-00008

    FDA Adverse Event
    Injury ·VITATRON MEDICAL B.V.·Product code NVY·February 15, 2013

    6000023-1997-00061

    FDA Adverse Event
    Injury ·September 10, 1997

    6000023-1999-00078

    FDA Adverse Event
    Injury ·November 12, 1999

    6000023-1999-00080

    FDA Adverse Event
    Injury ·November 12, 1999

    6000023-1999-00074

    FDA Adverse Event
    Injury ·November 12, 1999

    6000023-1999-00071

    FDA Adverse Event
    Injury ·November 12, 1999

    6000023-1999-00079

    FDA Adverse Event
    Injury ·November 12, 1999

    6000023-1999-00064

    FDA Adverse Event
    Injury ·September 8, 1999

    6000023-1999-00061

    FDA Adverse Event
    Injury ·September 8, 1999

    6000023-1999-00058

    FDA Adverse Event
    Injury ·September 8, 1999

    6000023-1999-00065

    FDA Adverse Event
    Injury ·September 8, 1999

    6000023-1999-00059

    FDA Adverse Event
    Injury ·September 8, 1999

    6000023-1999-00066

    FDA Adverse Event
    Injury ·September 8, 1999

    6000023-1999-00060

    FDA Adverse Event
    Injury ·September 8, 1999

    ENTERRA

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LNQ·February 19, 2020

    RINGLOC BI-POLAR CUP

    FDA Adverse Event
    Injury ·BIOMET, INC.·Product code JDI·January 18, 2008

    HEARTMATE 3 LVAS IMPLANT KIT

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·July 9, 2021

    FLIXENE SLIDER GDS

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORPORATION·Product code DSY·March 17, 2026