BEUDAMED
    35 results · 25ms · Sources: EU EUDAMED, US FDA

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    Bander Ureteral Diversion Stent Set, Dretler Ureteroscopy Stent Set

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    BANDER URETERAL DIVERSION STENT SET

    FDA Adverse Event
    Injury ·COOK INC·Product code FAD·June 14, 2023

    BANDER URETERAL DIVERSION STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·December 17, 2024

    BANDER URETERAL DIVERSION STENT SET

    FDA Adverse Event
    Injury ·COOK INC·Product code FAD·June 16, 2022

    BANDER URETERAL DIVERSION STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·July 11, 2024

    BANDER URETERAL DIVERSION STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·July 8, 2022

    BANDER URETERAL DIVERSION STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·March 19, 2024

    BANDER URETERAL DIVERSION STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·October 8, 2024

    BANDER URETERAL DIVERSION STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·January 28, 2021

    BANDER URETERAL DIVERSION STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·January 28, 2022

    DRETLER UNIVERSAL URETEROSCOPY STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·February 22, 2022

    BANDER URETERAL DIVERSION STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·February 9, 2022

    AccuQuest

    FDA UDI
    Bernafon AG·05711584078075·AQ CO9 MNR, 2.4G NFM PB SABE/MAC DEMO ACCUQ

    SYNTEC OS SPINAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BIOCLEAN CHEMO ULTIMATE POWDER FREE POLYCHLOROPRENE EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 21, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·July 28, 2011

    TENACULUM FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC.·Product code GCJ·September 22, 2008

    ACRYSOF IQ RESTOR SINGLEPIECE IOL

    FDA Adverse Event
    Malfunction ·ALCON RESEARCH, LLC - HUNTINGTON·Product code MFK·October 15, 2024

    ACRYSOF RESTOR TORIC SINGLEPIECE IOL

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LLC - HUNTINGTON·Product code MJP·October 11, 2024