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

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    ClariCT.AI

    FDA 510(k)
    FDA Class 2 ·Radiology

    Vanguard® Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00880304271210·

    Vanguard Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00880304466050·

    DIALOG WITH ADIMEA OPTION

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

    SYNERGY TISSUE MATRIX

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

    M2A ACETABULAR SYSTEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·April 19, 2017

    VANGUARD (TM) CR FEMORAL INTERLOK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018

    2183460-1996-00007

    FDA Adverse Event
    Injury ·Product code LSW·September 20, 1996

    2183460-1996-00004

    FDA Adverse Event
    Injury ·Product code LWS·September 20, 1996

    2183460-1996-00019

    FDA Adverse Event
    Injury ·Product code LWS·September 27, 1996

    2183460-1996-00012

    FDA Adverse Event
    Malfunction ·Product code LWS·September 6, 1996

    2183460-1996-00020

    FDA Adverse Event
    Injury ·Product code LWS·September 27, 1996

    2183460-1996-00017

    FDA Adverse Event
    Malfunction ·Product code LWS·September 13, 1996

    2183460-1996-00018

    FDA Adverse Event
    Malfunction ·Product code LWS·September 13, 1996

    2183460-1996-00006

    FDA Adverse Event
    Injury ·Product code LWS·September 20, 1996

    2183460-1996-00008

    FDA Adverse Event
    Malfunction ·Product code LWS·September 20, 1996

    2183460-1996-00009

    FDA Adverse Event
    Malfunction ·Product code LWS·September 20, 1996

    2183460-1997-00090

    FDA Adverse Event
    Injury ·Product code LWS·August 4, 1997

    2183460-1997-00091

    FDA Adverse Event
    Injury ·Product code LWS·August 4, 1997

    2183460-1997-00084

    FDA Adverse Event
    Injury ·Product code LWS·July 1, 1997