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 ×

    PNEUMATIC DEMAND OXYGEN CONSERVER (PDOC)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    INTRAUTERINE CATHETER TIP

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

    TempSure

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·March 5, 2013

    EP-4 STIMULATOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, AF DIVISION·Product code JOQ·February 8, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014