BEUDAMED
    10 results · 37ms · Sources: EU EUDAMED, US FDA

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    ATLANTIS Abutment for MIS Conical Connection Implants

    FDA 510(k)
    FDA Class 2 ·Dental

    HHM

    FDA UDI
    Oticon A/S·05707131343307·G100, MINIRITE T 312 2.4G C091 HHM

    CD HORIZON VOYAGER SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LIAISON XL ANALYZER MODEL 10050

    FDA 510(k)
    FDA Class 2 ·Microbiology

    NEXTAR INFRARED CAMERA

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code JWH·September 10, 2021

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 23, 2025

    ARTIS Q ZEEGO

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHINEERS AG·Product code OWB·December 10, 2024

    SAF-T-INTIMA SHIELDED IV CATHETER

    FDA Adverse Event
    Other ·BECTON DICKINSON INFUSION THERAPY SYSTEMS·Product code FOZ·October 8, 2008

    UNKNOWN M2A MAGNUM HIP

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 27, 2013

    POWERLINK SYSTEM

    FDA Adverse Event
    Injury ·ENDOLOGIX, INC.·Product code MIH·August 5, 2011