BEUDAMED
    202 results · 32ms · 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.

    SignalHF

    FDA UDI
    Implicity Inc.·03770025266015·

    ILR ECG Analyzer

    FDA UDI
    Implicity Inc.·03770025266008·

    SCHOLL FREEZE (WITH SHIELD) KIT

    FDA Adverse Event
    Injury ·ORASURE TECHNOLOGIES INC.·Product code GEH·October 19, 2016

    PROMED (INCLUDED IN CUSTOMED, INC. PACK)

    FDA Adverse Event
    Other ·PROMEDICAL PRODUCTS CO. LTD·Product code KKX·March 1, 2010

    DAVINCI XI

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·March 7, 2025

    DAVINCI XI

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·August 17, 2023

    DAVINCI XI

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·July 3, 2024

    CONSERVE HIP RESURFACER

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGIES INC·Product code KWA·July 19, 2012

    DAVINCI XI

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·September 29, 2023

    ENDOWRIST

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code GDW·April 4, 2024

    DAVINCI XI

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·July 17, 2024

    PLUS

    FDA Adverse Event
    Injury ·SMITH&NEPHEW, INC·Product code LPF·January 14, 2014

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·May 20, 2026

    ENDOWRIST

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·March 6, 2026

    DAVINCI XI

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·January 4, 2024

    VITROS IMMUNODIAGNOSTIC PRODUCTS TROPONIN I REAGENT PACK

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code MMI·May 24, 2007

    VITROS IMMUNODIAGNOSTIC PRODUCTS TROPONIN I REAGENT PACK

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code MMI·May 24, 2007

    NDI PASSIVE SPHERES

    FDA Adverse Event
    Malfunction ·NORTHERN DIGITAL, INC.·Product code HAW·July 11, 2014

    GORE® TAG® THORACIC BRANCH ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·November 5, 2025

    ZENITH FLEX AAA ENDOVASCULAR GRAFT BIFURCATED MAIN BODY

    FDA Adverse Event
    Injury ·COOK INC·Product code MIH·May 15, 2025