BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    CIRRUS HD-OCT

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    HHM

    FDA UDI
    Oticon A/S·05707131282507·H110V2, BTE 13 WL 85 STG HHM

    VESOFLOW

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PRE-POWDERED VINYL PATIENT EXAMINATION GLOVE, NON-STERILE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    FLEXTEND

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·July 6, 2011

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    JIANGSU YUYUE MEDICAL EQUIPMENT & SUPPLY CO., LTD·Product code IOR·June 6, 2013

    HS HAND CONTROLLED CURVED SHEAR

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC·Product code GEI·August 28, 2008

    ARTOURA BREAST TISSUE EXPANDER

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code LCJ·August 21, 2023