BEUDAMED
    9 results · 28ms · Sources: EU EUDAMED, US FDA

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    OsteoSeal Bone Hemostat

    FDA 510(k)
    FDA Unclassified ·Unknown

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517565907·CoRoent Ant TLIF PEEK, 14x12x34mm 8°

    31P/1H DUAL TUNED SURFACE COIL 3T; 23NA/ 1H DUAL TURNED SURFACE COIL 3T; 13C /1H DUAL TURNED SURFACE COIL 3T

    FDA 510(k)
    FDA Class 2 ·Radiology

    GRADIA DIRECT LOFLO

    FDA 510(k)
    FDA Class 2 ·Dental

    NOBLUS ULTRASOUND SCANNER

    FDA Adverse Event
    Malfunction ·Product code IYO·March 30, 2017

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 5, 2014

    PELVICOL ACELLULAR COLLAGEN MATRIX

    FDA Adverse Event
    Injury ·TISSUE SCIENCE LABORATORIES·Product code FTL·May 17, 2013

    TWINFIX TI 2.8 ANCHOR W/ULTRABRAID

    FDA Adverse Event
    Other ·SMITH & NEPHEW INC., ENDOSCOPY DIV.·Product code MBI·January 4, 2007

    Unify, Sterile EO, Model #/ Part #: CD3231-40/100029240, 100030104, 100041904; CD3231-40Q/100029281, 100030124, 100041905; CD3235-40/100029256, 100029293, 100029307, 100031111, 100037047, 100048897, 100070009; CD3235-40Q/100029257, 100029294, 100029308, 100031059, 100037048, 100070010; CD3281-40Q/100056770; CD3297-40/100056933

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018