BEUDAMED
    39 results · 21ms · Sources: EU EUDAMED, US FDA

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    MSA HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    REPICCI II RESURFACING KNEE SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304449879·

    Marienfeld Superior

    FDA UDI
    Paul Marienfeld GmbH & Co. KG·04250317300539·

    Tibial Keel Punch 3-4

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215056636·

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172973875·

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172973790·

    DURACON PS LIPPED TIBIAL INSERT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    POLY-TAPES (VARIOUS SIZES AND WOVEN CONSTRUCTION VARIANTS)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    SYNCHRON CREATINE KINASE REAGENT

    FDA Adverse Event
    BECKMAN COULTER INC.·Product code CGS·June 17, 2011

    LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code LDD·December 4, 2012

    LIFEPAK® 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·February 6, 2019

    2CM PERIPHERAL CUTTING BALLOON®

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code LIT·May 9, 2013

    INFINITI VISION SYSTEM

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·September 17, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 20, 2011

    LIFEPAK(R) 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·October 25, 2019

    M2A-MAGNUM 52-60MM TPR INSRT-6

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 26, 2013

    M2A-MAGNUM PF CUP 64ODX58ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 26, 2013

    M2A-MAGNUM 52-60MM TPR INS STD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 26, 2013

    M2A-MAGNUM PF CUP 62ODX56ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 26, 2013

    INTEGRAL/X LAT POR PROFILE 9MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·October 29, 2012