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

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    ARTAIRA Arterial Compression Device (AACD01)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Colibri Forcep

    FDA UDI
    Medetz Surgical Instruments LLC·G22312404990·Colibri Forcep 1x2 teeth, fenestrated handle OL...

    VERIFY V24 SELF-CONTAINED BIOLOGICAL INDICATOR FOR VAPORIZED VH202 STERILIZATION PROCESSES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    QuickDraw Venous Cannula

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 5/10 MM L E-CROSS

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·July 19, 2023

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·September 19, 2024

    QUICKSITE LV

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code OJX·September 9, 2011

    530G INSULIN PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·November 10, 2014

    1.0MM DRILL FOR 1.25MM SCREW

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HSZ·July 17, 2013