BEUDAMED
    12 results · 19ms · Sources: EU EUDAMED, US FDA

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    TRI-PHASIX CHROMATIC ALGINATE

    FDA 510(k)
    FDA Class 2 ·Dental

    X-CORE

    FDA UDI
    Nuvasive, Inc.·00887517270412·XC Mini Endcap, 17x14mm Contour Top Ø12

    P.F.C. SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295244226·P.F.C. SIGMA TIBIAL INSERT FIXED BEARING STABIL...

    AxoGuard Nerve Connector

    FDA 510(k)
    FDA Class 2 ·Neurology

    Q50 MEDICAL TREADMILL

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    HEARTSTART ONSITE

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 13, 2014

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM.

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·February 14, 2013

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·December 22, 2010

    CONTOUR ACETABULAR RECONSTRUCTION RING

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDJ·June 6, 2025

    MESH, SURGICAL, ACETABULAR, HIP, PROSTHESIS

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDJ·January 23, 2026

    AXOGUARD NERVE CONNECTOR AND PROTECTOR

    FDA Adverse Event
    Injury ·COOK BIOTECH·Product code JXI·October 24, 2019

    Depuy P.F.C. E Knee System, stabilized plus tibial insert; polyethylene tibial insert, Sz 4, 12.5 mm; Ref 96-2741.

    FDA Recall
    Terminated ·Depuy Orthopaedics, Inc.·Product code NJL·May 26, 2005