BEUDAMED
    10 results · 18ms · Sources: EU EUDAMED, US FDA

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    PRESS-FIT FLARED SHELL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    P.F.C. SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295233473·P.F.C. SIGMA TIBIAL COMPONENT ALL POLY CURVED 2...

    G3(TM) Active Plate(R) Small Fragment System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COHERENCE ONCOLOGIST WORKSPACE, MODEL 2.0 AND PHYSICIST WORKSPACE, MODEL 1.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code KWA·February 14, 2013

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·July 21, 2014

    UNICEL® DXC 880I SYNCHRON® ACCESS® CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHA·January 13, 2011

    Depuy P.F.C. E Knee System, all polyethylene curved tibial component, Sz 2.5, 15 mm; Ref 96-0633.

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

    MONOCRYL UD 27IN USP2-0

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAN·October 25, 2024

    MONOCRYL UD 27IN USP2-0

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAN·October 25, 2024