BEUDAMED
    7 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 ×

    PERITONEAL DIAL. TITA. CATH ADAPTER & LOCKING CAP

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    LOCKING TITANIUM ADAPTER

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·April 18, 2018

    DPS-3300 MICRO NUCLEAR MEDICINE IMAGING COMPUTER

    FDA 510(k)
    FDA Class 2 ·Radiology

    TRIGLYCERIDE'S TEST (TRIGLI-CINET)

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    PUMP, INFUSION, IMPLANTED, PROGRAMMABLE

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·June 25, 2014

    CAREASSIST BED

    FDA Adverse Event
    Malfunction ·HILL-ROM PLUVIGNER·Product code FNL·November 5, 2010

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·December 20, 2012