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

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    WALLSTENT ENDOPROSTHESIS

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

    Modulus

    FDA UDI
    Nuvasive, Inc.·00195377049940·Modulus ALIF Trial, 12x42x32mm 10°Lrg

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091982184·posteriors; shade D2 light; size XL; upper jaw

    Paper Sterilization Pouch and Roll(Sterilization Pouch Flat, Sterilization Pouch Gusseted, Sterilization Roll Flat and Sterilization Roll Gusseted)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    HR-1000 W/SUFFIXES (B,C OR D)

    FDA 510(k)
    FDA Class 1 ·Radiology

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·August 5, 2014

    LIGASURE IMPACT

    FDA Adverse Event
    Malfunction ·COVIDIEN LP (VALLEYLAB)·Product code GEI·January 18, 2011

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM

    FDA Adverse Event
    Injury ·BIOENTERICS CORPORATION·Product code LTI·November 19, 2007

    The Bigger Better-Bladder, Catalog Number BBB38 (with 3/8 inch ID tubing), Sterile, Single use only --- Manufactured for: Circulatory Technology Inc., 21 Singworth Street, Oyster Bay, 11771 (516) 624-2424 --- 510 (k) 981284.

    FDA Recall
    Terminated ·Circulatory Technology Inc·Product code DTN·June 3, 2009