BEUDAMED
    12 results · 24ms · Sources: EU EUDAMED, US FDA

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    PATHASSIST LIGHT SEEKER

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK, INC.·Product code MAX·May 9, 2019

    SMARTSET GHV GENTAMICIN BONE CEMENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PRECISION PORTABLE OXYGEN CONCENTRATION MODEL 4150

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CORNERSTONE-SR TI-COATED CAGE SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code ODP·October 11, 2018

    RESERVOIR 1.8ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·May 29, 2013

    SYMPHONY

    FDA Adverse Event
    Injury ·SORIN CRM·Product code NVZ·June 16, 2011

    ENDOWRIST PROGRASP INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC.·Product code GCJ·August 22, 2008

    CORNERSTONE-SR TI-COATED CAGE SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code ODP·September 7, 2017

    CORNERSTONE-SR® TI-COATED CAGE SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code ODP·October 6, 2025

    CORNERSTONE-SR® TI-COATED CAGE SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code ODP·October 8, 2024

    Achieva 1.5T

    FDA Enforcement
    Class II ·Ongoing·Philips North America Llc·November 29, 2023