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

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    Filters Regulation: Us FDA ×

    SonarMed AirWave Airway Monitoring System

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MULTIFUNCTION KEITO

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TSRH SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 22, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 27, 2013

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 22, 2014

    HANDLE ACETABULAR PRESS

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LXH·May 23, 2025

    ACETABULAR PRESSURIZER SMALL

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LXH·May 23, 2025

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·June 14, 2023