BEUDAMED
    31 results · 13ms · Sources: EU EUDAMED, US FDA

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    DiaSorin LIAISON HSV-2 Type Specific IgG, REF 310620

    FDA Recall
    Open, Classified ·Diasorin Inc.·Product code MYF·December 13, 2023

    Mobile airway scope-diagnosis and observation to access airway anatomy, endotracheal/endobronchial intubation and management. Model Numbers: MAF-DM2, MAF-GM, MAF-GM2, MAF-TM, MAF-TM2.

    FDA Recall
    Open, Classified ·Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan·Product code EOQ·September 25, 2023

    Olympus Airway Mobilescope, Models MAF-DM2, MAF-GM2, & MAF-TM2.

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code EOQ·July 27, 2023

    Cystonephroscope-endoscopic diagnosis and treatment within the bladder, urethra, and kidney Model Numbers: CYF-5, CYF-VH, CYF-VHR.

    FDA Recall
    Open, Classified ·Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan·Product code FAJ·September 25, 2023

    Olympus Airway Mobilescope, Models MAF-GM & MAF-TM.

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code EOQ·July 27, 2023

    Model No. CYF-5, Cystonephrofiberscope

    FDA Recall
    Open, Classified ·Shirakawa Olympus Co., Ltd. Azaokamiyama 3-1 Oazaodakura; Nishigo-Mura Nishishirakawa-Gun Japan·Product code FAJ·December 4, 2023

    Model No. CYF-5R, Cystonephrofiberscope

    FDA Recall
    Open, Classified ·Shirakawa Olympus Co., Ltd. Azaokamiyama 3-1 Oazaodakura; Nishigo-Mura Nishishirakawa-Gun Japan·Product code FAJ·December 4, 2023

    Olympus CYSTONEPHROFIBERSCOPE Model: CYF-5

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code FAJ·April 20, 2022

    Visera Hysterovideoscope Olympus HYF Type V

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code HIH·July 20, 2023

    Model No. CYF-VHR, CYSTO-NEPHRO VIDEOSCOPE

    FDA Recall
    Open, Classified ·Shirakawa Olympus Co., Ltd. Azaokamiyama 3-1 Oazaodakura; Nishigo-Mura Nishishirakawa-Gun Japan·Product code FAJ·December 4, 2023

    Model No. CYF-VH, CYSTO-NEPHRO VIDEOSCOPE

    FDA Recall
    Open, Classified ·Shirakawa Olympus Co., Ltd. Azaokamiyama 3-1 Oazaodakura; Nishigo-Mura Nishishirakawa-Gun Japan·Product code FAJ·December 4, 2023

    Model No. CYF-V2, VISERA Cysto-Nephro Videoscope

    FDA Recall
    Open, Classified ·Shirakawa Olympus Co., Ltd. Azaokamiyama 3-1 Oazaodakura; Nishigo-Mura Nishishirakawa-Gun Japan·Product code FAJ·December 4, 2023

    Model No. CYF-V2R, VISERA Cysto-Nephro Videoscope

    FDA Recall
    Open, Classified ·Shirakawa Olympus Co., Ltd. Azaokamiyama 3-1 Oazaodakura; Nishigo-Mura Nishishirakawa-Gun Japan·Product code FAJ·December 4, 2023

    Hysterofiberscope-For endoscopic diagnosis within the uterus. Model Number: HYF-XP.

    FDA Recall
    Open, Classified ·Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan·Product code EOQ·September 25, 2023

    Hysterovideoscope-For endoscopic diagnosis within the uterus Model Number: HYF-V.

    FDA Recall
    Open, Classified ·Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan·Product code HIH·September 25, 2023

    Hysteroscope-For endoscopic diagnosis within the uterus Model Number: HYF-1T.

    FDA Recall
    Open, Classified ·Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan·Product code HIH·September 25, 2023

    The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.

    FDA Recall
    Open, Classified ·IN MY BATHROOM LLC·Product code RHP·January 27, 2022

    ADVANTA VXT, 4-7X45, 1GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graft

    FDA Recall
    Open, Classified ·Atrium Medical Corporation·Product code DYF·May 3, 2024

    ADVANTA VXT, 5-8X45, 1GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graft

    FDA Recall
    Open, Classified ·Atrium Medical Corporation·Product code DYF·May 3, 2024

    ADVANTA VXT, 5X40, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft

    FDA Recall
    Open, Classified ·Atrium Medical Corporation·Product code DYF·May 3, 2024