BEUDAMED
    26 results · 7ms · Sources: EU EUDAMED, US FDA

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    Filters Classification: FDA Class 2 ×

    System, X-Ray, Tomography, Computed

    FDA classification
    FDA Class 2 ·System, X-Ray, Tomography, Computed

    C-DAK 3500

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

    MODIFIED C-DAK

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

    C-DAK ARTIFICIAL KIDNEY

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

    BAK-ON SP PORCELAIN ALLOY

    FDA 510(k)
    FDA Class 2 ·Dental

    ARTIFICIAL KIDNEY, C-DAK 0.6D

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

    KIDNEY, ARTIFICIAL, C-DAK 1.5

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    C-DAK 2100 ARTIFICIAL KIDNEY

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

    C-DAK 4000 ARTIFICIAL KIDNEY

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

    KIDNEY, ARTIFICIAL, C-DAK 2.0

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    ARTIFICIAL KIDNEY, C-DAK CORDIS DOW

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

    C-DAK DUO-FLUX ARTIFICIAL KIDNEY

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

    C-DAK TM 2800 ARTIFICIAL KIDNEY

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

    C-DAK DUO-FLUX ARTIFICIAL KIDNEY

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

    MODIFICATION TO BONE ANCHOR AND KIT (BAK)

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

    CORDIS DOW C-DAK 1.8MRC ARTIFIC-KIDNEY

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

    CORDIS DOW C-DAK 1.3MRC ARTIF. KIDNEY

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

    CleanCart A, CleanCart C, AK 98 Hemodialysis Machine

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

    AXYA MEDICAL INC, BONE ANCHOR SYSTEM AND KIT- (BAK)

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

    Ardis Interbody System, BAK Interbody Fusion System, BAK/C Anterior Cervical Interbody Fusion System, InFix Anterior Lumbar System, TraXis Vertebral Body Replacement (Ti and VUE)

    FDA 510(k)
    FDA Class 2 ·Orthopedic