BEUDAMED
    11 results · 26ms · Sources: EU EUDAMED, US FDA

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    MODIFIED COATRON II AND COATRON JR.

    FDA 510(k)
    FDA Class 2 ·Hematology

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377068408·RELINE C Screw, 5.0x6mm Occipital

    VERTEX® Reconstruction System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00721902060465·SCREW 6900506 VAS CANCELLOUS 3.5X6MM TI

    Trial Tibial Augment

    FDA UDI
    ADLER ORTHO SPA·08056269044134·TRIAL PANTHEON TIBIAL AUGMENT LM/RL SIZE 6 H5

    ZAVATION

    FDA UDI
    Zavation LLC·00842166151086·WHITNEY 12mmx14mm , 5deg , 06mm

    Master Series

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746135606·DB BKT MASTER UL CUSP 022 T-7 A+8 R=0

    BIO-FASTAK SUTURE ANCHOR, MODEL AR-1324B

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MAYFIELD INFINITY XR2 SKULL CLAMP, MODEL A-2114

    FDA 510(k)
    FDA Class 2 ·Neurology

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD .·Product code MCM·June 27, 2014

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 7, 2013

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·October 28, 2010