BEUDAMED
    2,286 results · 23ms · Sources: EU EUDAMED, US FDA

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    PIVOTEC LUMBAR INTERBODY FUSION DEVICE (LIFD)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DELTA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613252467519·DELTA 1.7MM FLEXIBLE MESH 122x122x0.5MM

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110928·STERILIZING CASE SINGLE VR

    Titan™

    FDA UDI
    Ascension Orthopedics, Inc.·10381780243151·Titan™ Total Shoulder System The Titan Modular ...

    VARISEED 7.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    RHIGENE MESACUP-2 TEST RNP, MODEL M7741

    FDA 510(k)
    FDA Class 2 ·Immunology

    INTUITIVE SURGICAL

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL·Product code NAY·December 9, 2015

    COROX OTW-S 85-BP

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code NKE·May 3, 2013

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, NEUROMODULATION·Product code GZB·August 27, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·May 18, 2011

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code OYC·May 31, 2017

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 14, 2017

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code OYC·May 26, 2017

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code OYC·May 26, 2017

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code OYC·May 26, 2017

    BIA400 IMPLANT 4MM W ABUTMENT 10MM

    FDA Adverse Event
    Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·October 9, 2017

    NUCLEUS 24 CONTOUR

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD·Product code MCM·February 8, 2017

    NUCLEUS FREEDOM IMPLANT WITH CONTOUR ADVANCE ELECTRODE

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code MCM·March 8, 2017

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code OYC·September 7, 2017

    GREENLIGHT HPS LASER SYSTEM

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·August 15, 2017