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

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    MAX-I-PROBE PERIODONTAL ENDODONTIC PROB

    FDA 510(k)
    FDA Class 1 ·Dental

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690199663·Modular Knee Stem Pilot 23mm x 75mm

    DISPOSABLE NEBULIZER SET

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    INTUITIVE SURGICAL DA VINCI ENDOSCOPIC INSTRUMENT CONTROL SYSTEM AND ENDOSCOPIC INSTRUMENTS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·November 20, 2012

    STERNALOCK BONE SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HRS·May 30, 2014

    ULTRAFLOW HPC 1.5F

    FDA Adverse Event
    Malfunction ·EV3 NEUROVASCULAR·Product code KRA·September 15, 2010