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

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    OSI RIZZOLI TRAUMA TABLE (ELECTRIC VERSION)

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Precept

    FDA UDI
    Nuvasive, Inc.·00887517431530·PRECEPT Screw, 10.5x60mm Fixed

    BURNSHIELD

    FDA UDI
    BURNSHIELD (PTY) LTD·06007645007641·BURNSHIELD DRESS CONTOUR 1X1M(40X40 )BAG

    Solitaire 2 and Solitaire Platinum Revascularization Device

    FDA 510(k)
    FDA Class 2 ·Neurology

    FERROFIBRE STAINLESS STEEL SUTURES, MODEL 610 SERIES SIZES (USP) 5-0 TO #5

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

    NexGen®

    FDA UDI
    Zimmer, Inc.·00889024200319·

    NexGen®

    FDA UDI
    Zimmer, Inc.·00889024200326·

    NexGen®

    FDA UDI
    Zimmer, Inc.·00889024200296·

    NexGen®

    FDA UDI
    Zimmer, Inc.·00889024200302·

    NexGen®

    FDA UDI
    Zimmer, Inc.·00889024200333·

    NexGen®

    FDA UDI
    Zimmer, Inc.·00889024200340·

    CONMED 5MM AUTOMATIC CLIP APPLIER

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code FZP·April 8, 2014

    COOL PATH DUO 7F, 1304-CP2-7-1.5(5)-L1-TE4BE1AB

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, IRVINE·Product code OAD·October 1, 2010

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·November 9, 2012

    Medtronic Sofamor Danek USA, CD Horizon Spinal System Agile Dynamic Stabilization Device, REF 7881060, 10mm, 5.5mm dia x 60mm, size: 10mm x 60mm, not for distribution in the U.S.A. or its territories, for spinal fixation.

    FDA Recall
    Terminated ·Medtronic Sofamor Danek USA Inc·Product code NQP·November 12, 2007

    BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026