BEUDAMED
    8 results · 23ms · 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 ×

    CORDIS AVANTI TRANS-RADIAL CATHETER SHEATH INTRODUCER KIT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    X-CORE

    FDA UDI
    Nuvasive, Inc.·00887517270429·XC Mini Endcap, 17x14mm 7° Lord Btm Ø12

    P.F.C. SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295244271·P.F.C. SIGMA TIBIAL INSERT FIXED BEARING STABIL...

    FERRITIN-LATEX, MODELS 1418-2070, 1418-0279

    FDA 510(k)
    FDA Class 2 ·Immunology

    Ontex and other proprietary names

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

    HEARTSTART ONSITE

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 13, 2014

    PORTABLE AIR COMPRESSOR FOR MEDICAL PURPOSES

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code BTI·February 14, 2013

    EON MINI RECHARGEABLE IPG

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION DIV.·Product code LGW·January 13, 2011