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

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    KNIGHT LIGHT NONLUBRICATED CONDOM

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    P.F.C. SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295233305·P.F.C. SIGMA TIBIAL INSERT FIXED BEARING TC3 5 ...

    EV1000 Clinical Platform with ClearSight Finger Cuff or ClearSight System, EV1000 Clinical Platform

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BC100 BODY COMPOSITION ANALYSIS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HUDSON SHERIDAN UNCUFFED TRACHEAL TUBE

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BTR·January 23, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·January 13, 2011

    QUICK COUPLING FOR K-WIRES

    FDA Adverse Event
    Malfunction ·Product code HWE·July 28, 2014

    Depuy P.F.C. E knee system, TC3 tibial insert; polyethylene tibial insert, Sz 5, 15.0 mm; Ref 96-0552.

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