BEUDAMED
    15 results · 22ms · Sources: EU EUDAMED, US FDA

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    Reprocessed ViewFlex Xtra ICE Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PROPELLER HEAD SCREW SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304269736·

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515026988·Brewster Ret, "E" 3/4" x 1 1/2", 8 3/4" length

    ARROW(R) NEXTSTEP TM ANTEGRADE CHRONIC HEMODIALYSIS CATHETER

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

    NEOMED POLYURETHANE FEEDING TUBE

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

    M2A-MAGNUM MODULAR HEAD SZ 56MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·October 17, 2014

    UNKNOWN DEPUY TIBIAL INSERT

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code JWH·June 21, 2013

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 27, 2015

    URETERAL BRUSH BIOPSY SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FDX·November 15, 2023

    CARTO 3 SYSTEM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·December 14, 2023

    URETERAL BRUSH BIOPSY SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FDX·January 7, 2022

    SFXSPI PDS+ UNI VIO 27IN 2-0 SA CT-1

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code NEW·January 23, 2025

    SFXSPI PDS+ UNI VIO 18IN 2-0 SA CT-1

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code NEW·January 23, 2025

    SFXSPI PDS+ UNI VIO 18IN 2-0 SA CT-1

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code NEW·January 23, 2025

    SFXSPI PDS+ UNI VIO 27IN 2-0 SA CT-1

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code NEW·January 23, 2025