BEUDAMED
    76 results · 32ms · Sources: EU EUDAMED, US FDA

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    iHealth Track Blood Pressure Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DIVERGENCE-L™ Anterior/Oblique Lumbar Fusion System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169502468·PLATE 2160014 ALIF PLATE 14MM

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694031165·1.7mm Cannulated Drill, Long, Quick Release

    Humeris Shoulder

    FDA UDI
    FX SOLUTIONS·03701037301593·HUMERIS STEM TA6V SIZE 14 CEMENTLESS Ti/HA

    MIRABAY

    FDA UDI
    Mirabay Orthodontics Corp.·05061075022668·KLEOS PSL METAL MBT 022 LL5 PK5

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707016908·CALIBRA 1ST MOLAR BANDS n.LR 14

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 12, 2020

    OHICHO3

    FDA Adverse Event
    Injury ·Product code LIT·July 19, 2019

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 14, 2020

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·September 30, 2020

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·May 28, 2020

    OHICHO3

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·September 26, 2018

    OHICHO3

    FDA Adverse Event
    Injury ·Product code LIT·September 17, 2019

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694067843·Cannulated 1.7mm Drill, Quick Release Long Ster...

    FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR, MODEL KD-557

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    INTELIFUSE, INC., WARMSYSTEM WITH STIMULINKS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OPTICROSS 18

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OBJ·March 28, 2025

    Stent, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·COBRA PzF NanoCoated Coronary Stent System

    OPTICROSS 18

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OBJ·August 6, 2025

    OPTICROSS 18

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OBJ·May 14, 2025