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

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    RESTORATION ACETABULAR WEDGE AUGMENTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169413658·BLADE 5102019 20MM WIDE VESSELBLADE 19CM

    RHEAD

    FDA UDI
    Stryker GmbH·00886385025001·Recon Stem Implant Plasma Coated, Size 2

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970010·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970027·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172974018·UniTip High Resolution Catheter 10F

    COLOR BUFFED (CB) DDH FEMORAL STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RETROGRADE CARDIOPLEGIA CANNULA, SELF-INFLATING, WITH MALLEABLE OR GUIDEWIRE STYLET

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HLM TUBING SET

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·April 1, 2015

    VKMO 70000 #QUADROX-I HMO 70000+VHK71

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTN·February 23, 2015

    BO-HQV 70600#ADULT PACK

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTN·February 19, 2015

    BO-HQV #70600ADULT PACK

    FDA Adverse Event
    Injury ·MAQUET CARDIOPULMONARY AG·Product code DTN·March 4, 2015

    BO-HQV 70600#ADULT PACK

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DWE·March 27, 2015

    BO-HQV 70600#ADULT PACK

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DWE·April 9, 2015

    VKMO 11000

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·February 24, 2015

    BO-HQV 70600 ADULT PACK

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTN·July 15, 2015

    RESERVOIR VHK

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTN·July 28, 2015

    VENOUS HARDSHELL CARDIOTOMY RESERVOIR

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTM·September 13, 2016

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC·Product code CBK·May 3, 2013

    9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 18, 2011