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.
    Filters Regulation: Us FDA ×

    MODEL PB3300 INTRA-ARTER BLOOD GAS MONIT SYS, MODI

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    LIMACORPORATE SMR CTA HUMERAL HEADS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Materialise Shoulder System™, Materialise Shoulder Guide and Models, SurgiCase Shoulder Planner

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PINNACLE MTL INS NEUT36IDX58OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·January 28, 2013

    PRIMUS/APOLLO

    FDA Adverse Event
    Malfunction ·DRAGER MEDICAL GMBH·Product code BSZ·November 3, 2010

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 14, 2014