BEUDAMED
    10,000 results · 749ms · Sources: EU EUDAMED, US FDA

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    MGC Diagnostics

    FDA UDI
    MEDICAL GRAPHICS CORPORATION·00810016251712·PREVENT II FILTER KIT-ROUND-WHITE-FN

    MGC Diagnostics

    FDA UDI
    MEDICAL GRAPHICS CORPORATION·00810016251705·PREVENT II FILTER KIT-ROUND-WHITE-FN

    MGC Diagnostics

    FDA UDI
    MEDICAL GRAPHICS CORPORATION·00810016251699·PREVENT II FILTER KIT-ROUND-WHITE-FN

    Zimmer Biomet Patient Specific Instruments

    FDA UDI
    Materialise NV·05420060310133·ZB CT TKA Zimmer Pin Guide and Bone Model kit

    Zimmer Biomet Patient Specific Instruments

    FDA UDI
    Materialise NV·05420060310126·ZB CT TKA Biomet Pin Guide kit

    Zimmer Biomet Patient Specific Instruments

    FDA UDI
    Materialise NV·05420060310119·ZB CT TKA Biomet Pin Guide and Bone Model kit

    Zimmer Biomet Patient Specific Instruments

    FDA UDI
    Materialise NV·05420060310140·ZB CT TKA Zimmer Pin Guide kit

    Zimmer Biomet Patient Specific Instruments

    FDA UDI
    Materialise NV·05420060310430·ZB CT TKA Biomet Spring Pin Guide and Bone Mode...

    Zimmer Biomet Patient Specific Instruments

    FDA UDI
    Materialise NV·05420060310461·ZB CT TKA Biomet Spring Pin Guide kit

    XCM BIOLOGIC TISSUE MATRIX

    FDA Adverse Event
    Malfunction ·KENSEY NASH CORP.·Product code FTM·November 16, 2012

    XCM BIOLOGIC TISSUE MATRIX

    FDA Adverse Event
    Malfunction ·KENSEY NASH CORP.·Product code FTM·April 9, 2012

    THROMCAT THROMBECTOMY CATHETER

    FDA Adverse Event
    Injury ·KENSEY NASH CORPORATION·Product code MCX·February 22, 2008

    TRIACTIV FX SPARE INFLATOR & SHIELDWIRE

    FDA Adverse Event
    Malfunction ·KENSEY NASH CORP.·Product code NFA·February 28, 2007

    THROMCAT THROMBECTOMY CATHETER

    FDA Adverse Event
    Malfunction ·KENSEY NASH CORP.·Product code DXE·December 1, 2006

    ThromCat Thrombectomy Catheter System. 7F 2.5 -7.0 mm 150 cm. Catalogue number 63000-01. It is a single-use, disposable device that is used to perform percutaneous maceration and removal of thrombus and restoration of blood flow.

    FDA Recall
    Terminated ·Kensey Nash Corp·Product code MCW·February 7, 2007

    ThromCat Thrombectomy Catheter System. Catalog number 63000-01

    FDA Recall
    Terminated ·Kensey Nash Corp·Product code MCW·May 21, 2007

    COPIOS BONE VOID FILLER - PASTE

    FDA Adverse Event
    Injury ·KENSEY NASH CORP.·Product code MQV·March 22, 2013

    COPIOS BONE VOID FILLER - PASTE

    FDA Adverse Event
    Injury ·KENSEY NASH CORP.·Product code MQV·March 22, 2013

    NEEDLELESS CONNECTOR W/ EXTENS

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FPA·July 13, 2016

    AFFINITY

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code KNC·June 2, 2021