BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    SYNTHES MINI LENGTHENING APPARATUS

    FDA 510(k)
    FDA Class 2 ·Dental

    artegral HD

    FDA UDI
    Merz Dental GmbH·D7091973018·posteriors; shade A2; size XS; upper jaw

    MDR17 Mobile Direct Radiographic System

    FDA 510(k)
    FDA Class 2 ·Radiology

    STEREOTACTIC TARGET POSITIONER, TARGET POSITIONER FOR LEKSELL HEADRING, STEREOTACTIC COUNTERWEIGHT

    FDA 510(k)
    FDA Class 2 ·Radiology

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·June 22, 2016

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024159068·

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024159075·

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024159082·

    ACCESS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - AIBONITO·Product code FPA·August 5, 2015

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·February 21, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 1, 2014