BEUDAMED
    26 results · 27ms · Sources: EU EUDAMED, US FDA

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    Cosmolock

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

    LIGHT SABER INTRODUCER NEEDLE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Diamond D

    FDA UDI
    Keystone Industries·H66810130401·Denture Acrylic HC Original Pwd

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040047804·Plugger Root Canal 11.5A

    CorticaLINK

    FDA UDI
    LINKSPINE, INC.·00817329020417·5.0mm Titanium Rod: 40mm Curved

    SLEEVED FILTER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    INTRASTENT PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY

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

    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

    VIBRANT SOUNDBRIDGE

    FDA Adverse Event
    Malfunction ·VIBRANT MED-EL HEARING TECHNOLOGY GMBH·Product code MPV·March 15, 2013

    SAPIEN XT TRANSCATHETER HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·August 15, 2014

    SPRINT FIDELIS

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code LWS·March 10, 2011

    UNKNOWN KUDO ELBOW

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

    BLOOD GROUPING REAGENT ANTI-K (KEL1)

    FDA Adverse Event
    Malfunction ·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code QHR·October 20, 2020