BEUDAMED
    593 results · 55ms · 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 ×

    CREATININE JAFFE GEN.2

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CGX·December 3, 2024

    NEEDLE INTEGRA 25X1 RB TW

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·March 10, 2021

    MAYFIELD INFINITY XR2 SKULL CLAMP

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code HBL·July 15, 2020

    MAYFIELD TRIAD SKULL CLAMP

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code HBL·November 20, 2019

    SILICONE PIP SZ. 1

    FDA Adverse Event
    Injury ·ASCENSION ORTHOPEDICS·Product code KYJ·November 26, 2019

    MCP DISPOSABLE PACK FOR STRYKER

    FDA Adverse Event
    Injury ·ASCENSION ORTHOPEDICS·Product code HTZ·November 26, 2019

    COBAS INTEGRA 400 PLUS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·May 14, 2013

    SILICONE PIP SZ. 0

    FDA Adverse Event
    Injury ·ASCENSION ORTHOPEDICS·Product code KYJ·November 26, 2019

    LIMITORR VOLUME LIMITING EVD 20 ML

    FDA Adverse Event
    Injury ·INTEGRA NEUROSCIENCES PR·Product code JXG·July 17, 2020

    IDRT, UNKNOWN

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES CORPORATION·Product code MDD·September 16, 2020

    IDRT, UNKNOWN

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES CORPORATION·Product code MDD·February 6, 2026

    SILICONE MCP SZ 20

    FDA Adverse Event
    Injury ·ASCENSION ORTHOPEDICS·Product code KYJ·November 26, 2019

    IDRT, UNKNOWN

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES CORPORATION·Product code MDD·July 13, 2022

    NPH LOW FLOW VALVE

    FDA Adverse Event
    Malfunction ·INTEGRA NEUROSCIENCES IMPLANTS S.A.·Product code JXG·April 28, 2005

    COBAS INTEGRA 400 PLUS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·September 9, 2025

    TINA-QUANT HEMOGLOBIN A1C GEN.3 - HEMOLYSATE AND WHOLE BLOOD APPLICATION

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LCP·May 5, 2025

    1823260-2017-00571

    FDA Adverse Event
    Malfunction ·March 16, 2017

    IDRT, UNKNOWN

    FDA Adverse Event
    Death ·INTEGRA LIFESCIENCES CORPORATION·Product code MDD·July 13, 2022

    IDRT, UNKNOWN

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES CORPORATION·Product code MDD·July 13, 2022

    CARPAL POLY, LARGE +1

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code JWJ·January 19, 2016