BEUDAMED
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    RELU BV

    FDA registration
    RELU BV·1 product·🇧🇪 Belgium

    Relu B.V.

    Manufacturer
    🇧🇪 Belgium·Kiwa Dare B.V.

    Relu B.V.

    Manufacturer
    🇧🇪 Belgium·1 Basic UDI-DI·1 Device

    Relu Creator

    Device
    EU MDR · Eu Md Class 2a ·Relu B.V.·On the market·32 countries

    Philips BV Endura, Rel. 2, 718074. Mobile C-Arm X-Ray systems offering Radiographic and Fluoroscopic techniques in a wide variety of applications.

    FDA Recall
    Terminated ·Philips Medical Systems North America Co. Phillips·Product code IXL·December 14, 2010

    Philips BV Pulsera, Rel. 2.3, 718095. Mobile C-Arm X-Ray systems offering Radiographic and Fluoroscopic techniques in a wide variety of applications.

    FDA Recall
    Terminated ·Philips Medical Systems North America Co. Phillips·Product code IXL·December 14, 2010

    Philips BV Libra, Mobile X-ray unit, 718022. Mobile C-Arm X-Ray systems offering Radiographic and Fluoroscopic techniques in a wide variety surgical and non-surgical applications including; cerebral, thoracic, abdominal, peripheral, orthopedic, cardiac, and vascular procedures.

    FDA Recall
    Terminated ·Philips Medical Systems North America Co. Phillips·Product code IZL·December 14, 2010

    Relu Creator

    Basic UDI-DI
    EU MDR · Eu Md Class 2a ·Relu B.V.·1 device

    MAGIC3¿ INTERMITTENT CATHETER WITH SURE-GRIP¿ SLEEVE

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code MJC·January 31, 2022

    MPA

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·June 16, 2008

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 20, 2008

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 20, 2008

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 24, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 15, 2008

    THUMPER

    FDA Adverse Event
    Malfunction ·MICHIGAN INSTRUMENTS, INC.·Product code DRM·July 14, 2005

    GE OEC 2600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·April 8, 2009

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 6, 2013

    CENTURY BED

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 24, 2009

    22M00047CRT01

    Certificate
    MDR QMS·Relu B.V.·Kiwa Dare B.V.

    8800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 10, 2013