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

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    PLEXOLONG SETS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0130140·Sagittal Bender, Right

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07311K0130110·Segmental Rod Reducer, Slim, Assembly

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07311K0100410·Caddie Lid, Curved Rods

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07311K0130400·ROD REDUCER, AXIAL

    SLT DIFFUSER FIBER

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ULTRASOUND SCANNER TYPE 2101

    FDA 510(k)
    FDA Class 2 ·Radiology

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDC·May 17, 2017

    DISC LT DSTL HMRL BDY SET

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDC·April 1, 2019

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDC·May 17, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDC·May 19, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDC·May 19, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDC·May 17, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Death ·BIOMET UK LTD.·Product code JDC·May 19, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDC·May 19, 2017

    WALLSTENT¿ RP ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code MAF·March 20, 2013

    ACCU-CHEK FLEXLINK PLUS

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code FRN·March 4, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 15, 2014

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDC·May 17, 2017

    XIENCE SKYPOINT¿

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR INC.·Product code NIQ·August 25, 2025