BEUDAMED
    5 results · 17ms · 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 ×

    COREVALVE TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·August 23, 2021

    URETEROSCOPE 6.9/8.4 FR. X 430 MM, 5°, STRAIGHT OCULAR, 3.7 FR. 2.6 FR. CHANNEL

    FDA Adverse Event
    Injury ·OLYMPUS WINTER & IBE GMBH·Product code FGB·December 4, 2024

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·February 15, 2011

    ZENITH RENU CONVERTER AAA ANCILLARY GRAFT

    FDA Adverse Event
    Injury ·COOK INCORPORATED·Product code MIH·February 21, 2008

    GMK-SPHERE FEMORAL COMPONENT SPHERE CEMENTED SIZE 5 L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 13, 2023