BEUDAMED
    16 results · 23ms · Sources: EU EUDAMED, US FDA

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    MaxBlend 2, MaxBlend Lite

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    THREADED STEINMANN PINS, TROCAR POINT

    FDA UDI
    Biomet Orthopedics, LLC·00887868016509·

    OSSEOCONDUCT

    FDA 510(k)
    FDA Class 2 ·Dental

    INNOVACON SPECTRUM II TEST CARD

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 8, 2024

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 24, 2025

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·February 19, 2019

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 11, 2013

    PORTEX 8.0MM VOCALAID TRACHEOSTOMY TUBE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL INTERNATIONAL LTD.·Product code JOH·March 29, 2011

    MX40 2.4 GHZ SMART HOPPING

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code DSI·July 23, 2014

    DTK FILTER, INTRAVASCULAR, CARDIOVASCULAR

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·February 19, 2019

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·February 19, 2019

    LUCAS 3 CHEST COMPRESSION SYSTEM

    FDA Adverse Event
    Death ·JOLIFE AB - 3005445717·Product code DRM·February 6, 2024

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·February 19, 2019

    LUCAS 3 CHEST COMPRESSION SYSTEM

    FDA Adverse Event
    Death ·JOLIFE AB - 3005445717·Product code DRM·February 6, 2024

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·March 23, 2018