BEUDAMED
    13 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Medline Sterile Water USP and Medline Sterile 0.9% Normal Saline USP

    FDA 510(k)
    FDA Unclassified ·Unknown

    CENTRONAIL TITANIUM UNIVERSAL FEMORAL NAILING SYSTEM

    FDA UDI
    ORTHOFIX SRL·18032937169245·RULER SUPPORT

    IONTOPHORESIS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    INTEL HEALTH GUIDE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACTIV.A.C.¿ THERAPY SYSTEM

    FDA Adverse Event
    Injury ·KINETIC CONCEPTS, INC.·Product code OMP·February 12, 2018

    BALL HEADS: COCR BALL HEAD 12/14 Ø 28 SIZE M 0

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JDI·September 6, 2024

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·June 7, 2013

    CONTAK RENEWAL

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·July 23, 2011

    LIFEVEST WCD 4000 SYS

    FDA Adverse Event
    Injury ·ZOLL MANUFACTURING CORPORATION·Product code MVK·September 23, 2014

    MPACT DOUBLE MOBILITY ACETABULAR SHELL 52

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·August 25, 2021

    ACTIV.A.C. ION PROGRESS REMOTE THERAPY MONITORING SYSTEM

    FDA Adverse Event
    Injury ·KINETIC CONCEPTS, INC.·Product code OMP·June 8, 2021

    ACTIV.A.C. ION PROGRESS REMOTE THERAPY MONITORING SYSTEM

    FDA Adverse Event
    Injury ·KINETIC CONCEPTS, INC.·Product code OMP·July 14, 2021

    LINER: MPACT DM DOUBLE MOBILITY HC LINER 28/DMG

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MEH·September 19, 2019