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

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    NEONATAL VENOUS HARDSHELL CARDIOTOMY RESERVOIR, PEDIATRIC VENOUS HARDSHELL CARSIOTOMY RESERVOIR, NEONATAL VENOUS HARDSHE

    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

    VENOUS HARDSHELL CARDIOTOMY RESERVOIR

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

    VKMO 78000

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTM·May 6, 2016

    VKMO 30000 # QUADROX - I PAD. MIT RESERVOIR

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTM·July 17, 2015

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169413740·BLADE 5102919 29MM WIDE VESSELBLADE 19CM

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964077265·Endo Carry-On Procedure Kit

    RESTORATION ACETABULAR WEDGE AUGMENTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PRO FOCUS 2202, PRO FOCUS 2202 UV MODEL: TYPE 2202

    FDA 510(k)
    FDA Class 2 ·Radiology

    LINEAR ST

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·April 10, 2019

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTN·May 9, 2013