BEUDAMED
    6 results · 26ms · 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.

    MONARCH STERILIZATION CONTAINER SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CARDIOLINE HD+

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Intracavitary/Interstitial System

    FDA 510(k)
    FDA Class 2 ·Radiology

    HEARTSTART XL + DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·March 17, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·November 26, 2012

    PROXIMATE PROCEDURE SET

    FDA Adverse Event
    ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 17, 2015