BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    Galaxy UNYCO System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODULAR DUAL MOBILITY LINER, X3 ACETABULAR INSERT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    POWDERED LATEX SURGICAL GLOVES STERILE, STERILE WITH PROTEIN CONTENT LABELING CLAIM

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code LZG·October 26, 2017

    REVO MRI SURESCAN

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWP·June 8, 2013

    ULTIMA ACTIVATOR II REUSABLE DRIVE MECH.

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC.·Product code DWS·June 17, 2011

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Injury ·ROCHE DIAGNOSIS·Product code LFR·September 4, 2008

    MYSPINE UNILATERAL LEFT GUIDE S01

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code PQC·August 22, 2024

    ELEKTA LIMITED Elekta Synergy, REF MRT 8501, MRT 8511; Medical Charged-Particle Radiation Therapy System Accelerator, Linear

    FDA Enforcement
    Class II ·Ongoing·Elekta, Inc.·December 13, 2023