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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    RECORDER, CHART, MODEL 5536

    FDA 510(k)
    FDA Class 1 ·Cardiovascular

    CLINICAL ELECTRONIC THERMOMETER, MODELS TP11403 THROUGH TP11413

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Ocata Anterior Cervical System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TX1 TISSUE REMOVAL SYSTEM - MICROTIP

    FDA Adverse Event
    Malfunction ·AOI, INC·Product code LFL·January 21, 2014

    LAP-BAND AP ADJUSTABLE GASTRIC BANDING SYSTEM (STANDARD)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·October 1, 2012

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWQ·July 21, 2010