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

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    ANSPAHC SPEED REDUCER

    FDA 510(k)
    FDA Class 2 ·Neurology

    P.F.C. SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295233442·P.F.C. SIGMA TIBIAL COMPONENT ALL POLY CURVED 2...

    SuperVu Galilean 3.0x, at 34cm working distance

    FDA UDI
    Rudolf Riester GmbH·04045396160620·Riester binocular loupes are used to enlarge th...

    Eye Shield

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111154·FOX EYE SHIELD GARTER ASST COLOR PK/50

    Invacare Platinum Mobile Oxygen Concentrator

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    REFLECTION 3-HOLE SHELL WITH ASYMMETRIC POROUS COATING

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    2800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 25, 2013

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code IOR·July 28, 2014

    CARPENTIER-EDWARDS PERIMOUNT MAGNA PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·January 13, 2011

    Depuy P.F.C. E Knee System, all polyethylene curved tibial component Sz 2.5, 8 mm; Ref 96-0630.

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

    Depuy P.F.C. E Knee System All Polyethylene Curved Tibial Component, 2.5, 8 mm, 67mm M/L, 45 mm A/P, UHMWPE, 2.5, sterile; Product Code/REF 96-0630.

    FDA Recall
    Terminated ·Depuy Orthopaedics, Inc.·Product code NJL·September 27, 2007