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

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    EVIDENCE PREGNANCY TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    P.F.C. SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295243977·P.F.C. SIGMA TIBIAL INSERT FIXED BEARING STABIL...

    Stimucel System, Stimucel Generator, Stimucel Treatment Wand, Stimucel Applicator

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

    GREENTON ECOLITE IPL SYSTEM

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

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 23, 2014

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·February 14, 2013

    QUATTRODE LEAD, 3/4MM, 60 CM

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL- NEUROMODULATION DIVISION·Product code LGW·January 13, 2011

    Depuy P.F.C. E Knee System, stabilized plus tibial insert; polyethylene tibial insert, Sz 2.5, 12.5 mm; Ref 96-2721.

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