BEUDAMED
    40 results · 23ms · Sources: EU EUDAMED, US FDA

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    FDA 510(k)
    FDA Class 2 ·Neurology

    1.5T 16-CHANNEL HAND-WRIST COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    ORTHODONTIC TAADS (TEMPORARY ANATOMICAL ANCHOR DEVICE SYSTEM)

    FDA 510(k)
    FDA Class 2 ·Dental

    GM HELIX ACQUA IMPLANT,TI,5.0X16

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·May 16, 2018

    GM HELIX IMPLANT 4.3X13

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·June 6, 2018

    GM HELIX IMPLANT 4.3X13

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·June 22, 2018

    GM DRIVE ACQUA IMPLANT 3.5X8 MM

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·August 29, 2018

    GM HELIX ACQUA IMPLANT 3.75X11.5

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·April 24, 2018

    ZILVER 518 BILIARY SELF-EXPANDING STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·September 21, 2017

    GM HELIX IMPLANT 3.5X10

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·June 29, 2018

    ZILVER 635 BILIARY SELF-EXPANDING STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·September 20, 2017

    ZILVER 635 SELF-EXPANDING BILIARY STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·September 7, 2017

    ZILVER 635 SELF-EXPANDING BILIARY STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FGE·February 28, 2018

    ZILVER 635 BILIARY SELF-EXPANDING STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FGE·February 12, 2018

    SERVO-I

    FDA Adverse Event
    Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·June 15, 2023

    GM HELIX ACQUA IMPLANT 3.5X11.5

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·April 24, 2018

    GM DRIVE IMPLANT 3.5X10

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·April 20, 2018

    HANCOCK 2 VALVE

    FDA Adverse Event
    Death ·MEDTRONIC·Product code DYE·October 6, 2014

    UNKNOWN DEPUY ASR FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KXA·July 8, 2011

    SIMPLEX P-JAPANESE TWIN PACK

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LOD·June 11, 2013