BEUDAMED
    2,117 results · 36ms · Sources: EU EUDAMED, US FDA

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    EUREKA COLLIMATOR

    FDA Adverse Event
    Malfunction ·MIDMARK CORPORATION·Product code IZW·January 22, 2010

    LINEAR III

    FDA Adverse Event
    Malfunction ·PROGENY, INC.·Product code IZW·March 19, 2002

    ULTRANET S

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS S.C.S.·Product code IZW·May 30, 2007

    EUREKA LINEAR III

    FDA Adverse Event
    Injury ·PROGENY, INC.·Product code IZW·November 8, 2000

    MIDMARK/PROGENY

    FDA Adverse Event
    Malfunction ·QUANTUM MEDICAL IMAGING, LLC.·Product code IZW·September 17, 2014

    RALCO COLLIMATOR IN XPLORER 1590 SYSTEM

    FDA Adverse Event
    Malfunction ·RALCO INC·Product code IZW·November 27, 2006

    EUREKA COLLIMATOR

    FDA Adverse Event
    Malfunction ·MIDMARK CORPORATION·Product code IZW·June 23, 2011

    LINGAR COLLIMATOR

    FDA Adverse Event
    Malfunction ·PROGENY, INC·Product code IZW·July 2, 2007

    COLLIMATOR, AUTOMATIC, RADIOGRAPHIC

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHINEERS·Product code IZW·December 13, 2024

    R-30H , Diagnostic X-Ray Beam-Limiting Device. In combination with any of below X-ray tubes 0.6/1.2P364DK-85, 0.6/1.2P324DK-125, 0.6/1.2P324DK-85, 0.6/1.2P38DE-85 Device Model # R-30H. Subsequent Product Code: IZX Product Usage: The device is the beam-limiting device for X-ray Radiography.

    FDA Recall
    Terminated ·Shimadzu Medical Systems·Product code IZW·October 28, 2011

    Philips Collimators, Model numbers: 9896 010 00614, 9896 010 00615, 9804 607 00301, and 9804 602 83501. Product is a Collimator/ Beam Limiting Device and are replacement components for the Bucky Diagnost TH X-ray system.

    FDA Recall
    Terminated ·Philips Medical Systems North America Co. Phillips·Product code IZW·March 15, 2007

    Philips Gallileo Automatic Collimator, Part Numbers: 9896 010 00612, 9896 010 00614, 9896 010 00615. The device is a diagnostic x-ray beam-limiting device intended to restrict the dimensions of a diagnostic x-ray field by limiting the size of the primary x-ray beam.

    FDA Recall
    Terminated ·Philips Medical Systems North America Co. Phillips·Product code IZW·February 7, 2008

    Collimator, Automatic, Radiographic

    FDA classification
    FDA Class 2 ·Collimator, Automatic, Radiographic

    ITW FILTERTEK

    FDA registration
    ITW FILTERTEK·1 product·🇺🇸 United States

    WASE WERKPLAATS VZW

    FDA registration
    WASE WERKPLAATS VZW·1 product·🇧🇪 Belgium

    IZI MEDICAL PRODUCTS LLC

    FDA registration
    IZI MEDICAL PRODUCTS LLC·16 products·🇺🇸 United States

    OPTIMAT (AFDELING HUIZE TORDALE VZW)

    FDA registration
    OPTIMAT (AFDELING HUIZE TORDALE VZW)·1 product·🇧🇪 Belgium

    Easy@Home Disposable Plastic Urine Cup (100- pack)

    FDA UDI
    EASY HEALTHCARE CORPORATION·00855944007369·100 Disposable Plastic Urine Specimen Cups

    Western/Scott Fetzer

    FDA UDI
    Western Enterprises·B929BZW19550·SP "E" SZ MNS-603 w/WHITE CYL

    Easy@Home Disposable Plastic Urine Specimen Cups (50- pack)

    FDA UDI
    EASY HEALTHCARE CORPORATION·00855944007352·50 Disposable Plastic Urine Specimen Cups