BEUDAMED
    12 results · 19ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    SWAN NECK PRESTERNAL PERITONEAL DIALYSIS CATHETER

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

    Acetabular reamer ø42mm

    FDA UDI
    Incipio Devices SA·07630055302687·Acetabular reamer for hip arthroplasty

    System, Imaging, Fluorescence

    FDA Pre-Market Approval
    FDA Class 3 ·PINPOINT ENDOSCOPIC LIGHT SOURCE AND VIDEO CAMERA

    PleuraFlow System

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    WU'S 4-WHEELED NEO SCOOTER, WT-XL4

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    System, Imaging, Fluorescence

    FDA Pre-Market Approval
    FDA Class 3 ·ONCO-LIFE ENDOSCOPIC LIGHT SOURCE AND VIDEO CAMERA (ONCO-LIFE)

    System, Imaging, Fluorescence

    FDA Pre-Market Approval
    FDA Class 3 ·XILLIX-LIFE-LUNG

    System, Imaging, Fluorescence

    FDA Pre-Market Approval
    FDA Class 3 ·PINPOINT ENDOSCOPIC LIGHT SOURCE AND VIDEO CAMERA

    System, Imaging, Fluorescence

    FDA Pre-Market Approval
    FDA Class 3 ·PINPOINT ENDOSCOPIC LIGHT SOURCE AND VIDEO CAMERA

    ITREL 3

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·February 8, 2013

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·January 6, 2011

    GRANUFLO

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 27, 2014