BEUDAMED
    10,000 results · 74ms · Sources: EU EUDAMED, US FDA

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    SURGICAL INSTRUMENT

    FDA UDI
    Sin Sistema de Implante Nacional S/A·07899995208675·DRILL LANCE Ø2.0X18

    INSTRUMENT

    FDA UDI
    Sin Sistema de Implante Nacional S/A·07899995242754·DRILL LANCE Ø2.0MM

    Pinnacle

    FDA UDI
    Harmar Summit, LLC·00817650026126·Leaflift Stairlift Folding Rail Left Hand

    DUODENOVIDEOSCOPE

    FDA Adverse Event
    Death ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDT·November 26, 2020

    DUODENOVIDEOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDT·November 26, 2020

    DUODENOVIDEOSCOPE

    FDA Adverse Event
    Death ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDT·November 25, 2020

    DUODENOVIDEOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDT·November 26, 2020

    DUODENOVIDEOSCOPE

    FDA Adverse Event
    Death ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDT·November 26, 2020

    DAVINCI 5

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·May 7, 2026

    DAVINCI XI

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·August 23, 2023

    DAVINCI XI

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·January 5, 2024

    DAVINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·June 10, 2023

    DAVINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·December 8, 2023

    DAVINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·January 5, 2026

    DAVINCI 5

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·January 28, 2025

    Boston Scientific brand pull Gastro-dome (percutaneous endoscopic gastrostomy tubes) Kit, 20 Frl; catalog number 6838.

    FDA Recall
    Terminated ·Boston Scientific Corp·Product code KNT·June 2, 2005

    Boston Scientific brand pull Gastro-dome (percutaneous endoscopic gastrostomy tubes) Kit, 24 Frl; catalog number 6839.

    FDA Recall
    Terminated ·Boston Scientific Corp·Product code KNT·June 2, 2005

    13CM(5") APPX 0.37ML,SMALLBORE EXT SET W/PRE-PIERCED T-CONNECTOR,CLAMP,LUER SLIP

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FMG·November 10, 2023

    DAVINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·March 25, 2026

    DAVINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·May 4, 2026