BEUDAMED
    26 results · 49ms · Sources: EU EUDAMED, US FDA

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    LIFELINE MEDICAL, INC.

    FDA registration
    LIFELINE MEDICAL, INC.·3 products·🇺🇸 United States

    NRG TRANSSEPTAL NEEDLE

    FDA Adverse Event
    Injury ·BAYLIS MEDICAL COMPANY INC.·Product code DXF·December 21, 2022

    NRG TRANSSEPTAL NEEDLE

    FDA Adverse Event
    Injury ·BAYLIS MEDICAL COMPANY INC.·Product code DXF·December 23, 2022

    EZ STEER¿ THERMOCOOL® NAV BI-DIRECTIONAL CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code OAD·January 7, 2011

    RELAY PRO THORACIC STENT-GRAFT SYSTEM

    FDA Adverse Event
    Injury ·BOLTON MEDICAL, INC·Product code MIH·June 27, 2025

    RELAY PRO THORACIC STENT-GRAFT SYSTEM

    FDA Adverse Event
    Malfunction ·BOLTON MEDICAL, INC.·Product code MIH·February 18, 2025

    NRG TRANSSEPTAL NEEDLE

    FDA Adverse Event
    Injury ·BAYLIS MEDICAL COMPANY INC.·Product code DXF·December 21, 2022

    CARESITE® (LAD) SYSTEM

    FDA Adverse Event
    Injury ·B. BRAUN MEDICAL INC.·Product code FPA·April 11, 2016

    GENERIC - LASSO

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (IRWINDALE)·Product code DRF·September 30, 2016

    GENERIC - LASSO

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (IRWINDALE)·Product code DRF·September 30, 2016

    GENERIC - LASSO

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (IRWINDALE)·Product code DRF·September 30, 2016

    GENERIC - LASSO

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (IRWINDALE)·Product code NLH·September 30, 2016

    GENERIC - LASSO

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (IRWINDALE)·Product code DRF·September 30, 2016

    15 ELECTRODE DBL. INSULATED SPATULA TIP

    FDA Adverse Event
    Malfunction ·LIFE LINES MEDICAL, INC.( LIFE INSTRUMENT CORP.)·Product code KNF·August 30, 2004

    RELAY PRO NBS THORACIC STENT-GRAFT SYSTEM

    FDA Adverse Event
    Malfunction ·BOLTON MEDICAL, INC.·Product code MIH·April 18, 2024

    GORE® DRYSEAL FLEX INTRODUCER SHEATH

    FDA Adverse Event
    Malfunction ·W. L. GORE & ASSOCIATES, INC.·Product code DYB·September 5, 2023

    RELAY PRO NBS THORACIC STENT-GRAFT SYSTEM

    FDA Adverse Event
    Malfunction ·BOLTON MEDICAL INC.·Product code MIH·September 25, 2023

    RELAY PRO NBS THORACIC STENT-GRAFT SYSTEM

    FDA Adverse Event
    Injury ·BOLTON MEDICAL, INC.·Product code MIH·December 23, 2025

    GORE® EXCLUDER® AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·September 29, 2023

    OPTIMA COIL SYSTEM

    FDA Adverse Event
    Malfunction ·BALT USA·Product code HCG·November 7, 2024