BEUDAMED
    32 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Nerve Capping Device

    FDA 510(k)
    FDA Class 2 ·Neurology

    XELIS DENTAL

    FDA 510(k)
    FDA Class 2 ·Radiology

    MONT BLANC PEDICLE SCREW SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·June 10, 2020

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·RICE CREEK MFG·Product code DXY·June 7, 2013

    7700

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·June 24, 2011

    AXSYM RUBELLA IGG ANTIBODY

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code LFX·September 10, 2008

    CD HORIZON® FENESTRATED SCREW SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·September 3, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 25, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 25, 2024

    MERGE HEMO

    FDA Adverse Event
    Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

    CD HORIZON® SOLERA¿ FENESTRATED SCREW SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code NKB·July 28, 2025

    CD HORIZON® SOLERA¿ FENESTRATED SCREW SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code NKB·July 28, 2025