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

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    APOLLO TOTAL KNEE SYSTEM SINGLE LUG PATELLA

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    P.F.C. SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295233176·P.F.C. SIGMA TIBIAL INSERT FIXED BEARING TC3 3 ...

    MEGA PLUS MIS SPINE SYSTEM

    FDA UDI
    BK MEDITECH CO.,LTD.·08809665584014·MIS Cannulated Screw, Ø10.5 x 35mm, Ø6.0mm Rod

    N/A

    FDA UDI
    MEDTRONIC NAVIGATION, INC.·00681490915939·ADAPTER 960-535 ACC MNT DBL STARBURST

    N/A

    FDA UDI
    MEDTRONIC NAVIGATION, INC.·00763000055554·ADAPTER 960-535 ACC MNT DBL STARBURST

    N/A

    FDA UDI
    MEDTRONIC NAVIGATION, INC.·00763000379049·ACC 960-535 MNT DOUBLE STAR ADPTR-MAY

    N/A

    FDA UDI
    MEDTRONIC NAVIGATION, INC.·00763000251703·ACC 960-535 MNT DOUBLE STAR ADPTR-MAY

    N/A

    FDA UDI
    MEDTRONIC NAVIGATION, INC.·00763000337148·ACC 960-535 MNT DOUBLE STAR ADPTR-MAY

    UNILATERAL OXYGEN DELIVERY SYSTEM (ULODS)

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    SPACER-S TEMPORARY SHOULDER SPACER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACC 960-535 MOUNT DOUBLE STAR ADAPTER

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·March 19, 2019

    IAB: 7.5FR - 40 CC

    FDA Adverse Event
    Injury ·ARROW INTL., INC.·Product code DSP·February 12, 2013

    DARCO(R) LOCKING SCREW

    FDA Adverse Event
    Malfunction ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code HRS·January 13, 2011

    UNKNOWN DEPUY MED FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·July 28, 2014

    Depuy P.F.C. E knee system, TC3 tibial insert; polyethylene tibial insert, Sz 3, 22.5 mm; Ref 96-0535.

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