BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    REPLACEMENT BATTERIES PART NO. 5098,5135, 5097

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    OMNI Knee

    FDA UDI
    Omni Life Science, Inc.·00841690101505·Ultra Tibial Insert CS, Size 1 x 18mm

    LP Low Profile

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746091469·DB BKT LP V-SLOT LR CUSP 018 T-3 A+6 R3M

    NA

    FDA UDI
    Zimmer, Inc.·00889024104341·

    VAGINAL CONTINENCE DEVICE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    CRYSTAL ENTERIC/NONFERMENTER ID SYSTEM

    FDA 510(k)
    FDA Class 1 ·Microbiology

    ULTRACISION HARMONIC ACE

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

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·January 30, 2013

    POLYHESIVE PATIENT RETURN ELECTRODE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code GEI·December 22, 2010

    OMNILINK ELITE PERIPHERAL STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIO·July 15, 2014