BEUDAMED
    6 results · 18ms · 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.

    MUELLER-HINTON AGAR

    FDA 510(k)
    FDA Class 2 ·Microbiology

    STENT GRAFT BALLOON CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    F&P Nivairo RT047 Vented Hospital Full Face Mask, Anti-Asphyxiation Valve Version

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 6, 2014

    EXTERNAL PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA INC.·Product code DTE·October 15, 2012

    CAPSUREFIX

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 10, 2010