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

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    ML MICROKERATOME

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981071·anteriors; shade A3; mould IM2

    Gen. Acces/ Instr. Tip Guard

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112335·SURG-I-BAND LIME GREEN

    SIRA RFA Electrosurgical Device

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

    SYNTHES 6.5MM MIDFOOT FUSION BOLT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·March 17, 2016

    DEXTRUS 4136

    FDA Adverse Event
    Injury ·BIOTORNIK SE & CO. KG·Product code NVZ·February 19, 2013

    SIGMA 300 DR

    FDA Adverse Event
    Death ·MEDTRONIC MED REL, INC.·Product code DXY·February 8, 2011

    2800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 24, 2014