BEUDAMED
    31 results · 26ms · Sources: EU EUDAMED, US FDA

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    MEDIGUIDE TECHNOLOGY

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DULEX

    FDA UDI
    Davol Inc.·00801741011894·Bard Dulex Mesh

    EVOTECH™

    FDA UDI
    ADVANCED STERILIZATION PRODUCTS SERVICES INC.·10705037067220·Connector Tube, White and Green

    LOCATOR R-Tx

    FDA UDI
    Zest Anchors, LLC·00840481133695·LOCATOR R-Tx Abutment, Keystone Conical, 1mm Cuff

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450093894·

    Innomed, Inc.

    FDA UDI
    INNOMED, INC.·00840277115072·J-Hook Extractor for Femoral Stem without Slaph...

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K1230010·Rod Holder, Straight, 5.5 mm

    MODIFICATION TO VISTA STEREOSCOPE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    OPAL BOND FLOW

    FDA 510(k)
    FDA Class 2 ·Dental

    OPEN SPINE CLAMP, TITANIUM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC.·Product code HAW·February 26, 2014

    ACCESS TOTAL T4 CALIBRATOR

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code KLI·January 3, 2012

    UNKNOWN PRODUCT - SET SCREW

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HWC·October 12, 2012

    CONMED HAND CONTROLLED BOVIE

    FDA Adverse Event
    CONMED·Product code GEI·November 29, 2012

    BIPOLAR INSERT CEV634-1A 350MM MOUIEL

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INSTRUMENTATION S.A.S.·Product code GEI·August 29, 2013

    NEEDLE HOLDER CEV500T5 DIA 5MM TUNGSTEN

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INSTRUMENTATION S.A.S.·Product code GCJ·August 29, 2013

    BIPOLAR INSERT CEV633-1A 350MM BOTELLA

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INSTRUMENTATION S.A.S. LE PAVILLON·Product code GEI·August 29, 2013

    TUBE CEV64-5B DIA 5MM 350MM

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INSTRUMENTATION S.A.S.·Product code GEI·August 29, 2013

    OBTRYX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·May 20, 2013

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·September 26, 2014

    ZENITH FLEX AAA ENDOVASCULAR GRAFT BIFURCATED MAIN BODY

    FDA Adverse Event
    Injury ·COOK, INC.·Product code MIH·June 2, 2011