BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    VITAL SIGNS MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NexxZr™ T / D-100-16-NT-A350-SD

    FDA UDI
    SAGEMAX BIOCERAMICS, INC·00842271112477·

    AUTOSURE VOICE II BLOOD GLUCOSE MONITORING SYSTEM AND TEST STRIPS

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CD HORIZON (ADDITION OF SPINOUS PROCESS PLATE)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 4, 2024

    ASKU

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA INC.·Product code DTE·June 16, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·October 1, 2014

    UNKNOWN SUSPENSORY FIXATION DEVICE

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBI·July 13, 2023

    UNKNOWN SUSPENSORY FIXATION DEV

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBI·July 10, 2023

    UNKNOWN SUSPENSORY FIXATION DEVICE

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBI·July 17, 2023