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

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    OMNIPULSE/OMNIPULSE-MAX

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

    P.F.C. SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295243564·P.F.C. SIGMA TIBIAL COMPONENT ALL POLY STABILIZ...

    INSALL/BURSTEIN(TM)* II TIBIAL WEDGES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GAS-LYTE 1CC AND 3CC ARTERIAL BLOOD SAMPLERS

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR PURITAN·Product code CBK·June 18, 2014

    XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·February 14, 2013

    TRUFILL DCS ORBIT DETACHABLE COILS COMPLEX

    FDA Adverse Event
    Malfunction ·CORDIS NEUROVASCULAR, INC.·Product code HCG·January 18, 2011

    Depuy P.F.C. E Knee System, stabilized all-polyethylene tibia, Sz 2.5, 12.5 mm; Ref 96-2632.

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