BEUDAMED
    24 results · 29ms · Sources: EU EUDAMED, US FDA

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    CoLink™ Afx Plating System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Halyard

    FDA UDI
    Avanos Medical, Inc.·10680651929478·

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515025127·Murphy Ret, 7 3/4", 6 prong, sharp

    GUARDIAN II NC HEMOSTASIS VALVE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    COOK AND COOK SPECTRUM CENTRAL VENOUS CATHETERS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BD PLASTIPAK¿ CENTRIC LUER-LOCK HYPODERMIC THREE-PIECE SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·June 13, 2022

    Arietta 850 Ultrasound- Software Version: V1.0.0 through V4.1.3

    FDA Enforcement
    Class II ·Ongoing·FujiFilm Healthcare Americas Corporation·November 10, 2021

    5.0 CM SHORT ATTACHMENT

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·October 17, 2014

    TRANSFER SET

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·June 20, 2013

    SYNVISC ONE (HYLAN G-F 20) INJECTION 6/ML

    FDA Adverse Event
    Injury ·GENZYME BIOSURGERY (RIDGEFIELD)·Product code MOZ·July 22, 2011

    NSK

    FDA Adverse Event
    Malfunction ·NAKANISHI INC.·Product code EFB·December 6, 2018

    BD PLASTIPAK¿ LUER-LOK¿ TIP SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·November 1, 2021

    CATHETER, INTRAVASCULAR, THERAPEUTIC, SHORT-TERM LESS THAN 30 DAYS

    FDA Adverse Event
    Injury ·COOK INC·Product code FOZ·August 22, 2022

    CATHETER, INTRAVASCULAR, THERAPEUTIC, SHORT-TERM LESS THAN 30 DAYS

    FDA Adverse Event
    Injury ·COOK INC·Product code FOZ·August 22, 2022

    TRIPLE LUMEN POLYURETHANE CENTRAL VENOUS CATHETER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQY·July 3, 2018

    TRIPLE LUMEN POLYURETHANE CENTRAL VENOUS CATHETER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQY·July 3, 2018

    TRIPLE LUMEN POLYURETHANE CENTRAL VENOUS CATHETER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQY·June 25, 2018

    Catheter, intravascular, therapeutic, short-term less than 30 days

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FOZ·November 10, 2022

    1820334-2022-00399

    FDA Adverse Event
    Injury ·COOK INC·Product code LJS·March 16, 2022

    AquaC UNO H [120V, 60Hz, 1000VA, Fresenius US-Version: 24-10VA-1 Vivonic Part Number: G02000970-US

    FDA Enforcement
    Class II ·Ongoing·Fresenius Medical Care Holdings, Inc.·August 3, 2022