BEUDAMED
    12 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Death ×

    LOTUS EDGE VALVE SYSTEM

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC CORPORATION·Product code NPT·November 2, 2020

    GORE® EXCLUDER® CONFORMABLE AAA ENDOPROSTHESIS

    FDA Adverse Event
    Death ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·November 11, 2021

    GORE® DRYSEAL FLEX INTRODUCER SHEATH

    FDA Adverse Event
    Death ·W. L. GORE & ASSOCIATES, INC.·Product code DYB·November 11, 2021

    HEARTMATE

    FDA Adverse Event
    Death ·2CI·Product code DWB·February 6, 1997

    BCI

    FDA Adverse Event
    Death ·BCI INTERNATIONAL·Product code DQA·July 2, 1999

    BCI

    FDA Adverse Event
    Death ·SIMMS BCI·Product code DQA·August 22, 2001

    *

    FDA Adverse Event
    Death ·BCI, INC.·Product code DQA·September 6, 2001

    BCI PULSE PATIENT CABLE

    FDA Adverse Event
    Death ·SIMS BCI, INC·Product code DSA·December 4, 2002

    BCI

    FDA Adverse Event
    Death ·SMITHS MEDICAL PM, INC.·Product code DQA·June 7, 2004

    BIOMET CC I-BEAM TRAY

    FDA Adverse Event
    Death ·ZIMMER BIOMET, INC.·Product code JWH·August 6, 2018

    BIOMET CC I-BEAM TRAY 75MM

    FDA Adverse Event
    Death ·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018

    BIOMET CC I-BEAM TIBIAL TRAY 71MM

    FDA Adverse Event
    Death ·ZIMMER BIOMET, INC.·Product code JWH·August 6, 2018