BEUDAMED
    176 results · 21ms · Sources: EU EUDAMED, US FDA

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    Stent, Carotid

    FDA Pre-Market Approval
    FDA Class 3 ·Neuroguard IEP® 3-in-1 Carotid Stent, Post-Dilation Balloon System with Integrated Embolic Protection

    Stent, Carotid

    FDA Pre-Market Approval
    FDA Class 3 ·Neuroguard IEP® 3-in-1 Carotid Stent and Post-Dilation Balloon System with Integrated Embolic Protection – (Neuroguard I

    Stent, Carotid

    FDA Pre-Market Approval
    FDA Class 3 ·Neuroguard IEP® 3-in-1 Carotid Stent, Post-Dilation Balloon System with Integrated Embolic Protection

    Stent, Carotid

    FDA Pre-Market Approval
    FDA Class 3 ·Neuroguard IEP® 3-in-1 Carotid Stent and Post- Dilatation Balloon System with Integrated Embolic Protection

    Stent, Carotid

    FDA Pre-Market Approval
    FDA Class 3 ·Neuroguard IEP® 3-in-1 Carotid Stent and Post- Dilatation Balloon System with Integrated Embolic Protection

    Stent, Carotid

    FDA Pre-Market Approval
    FDA Class 3 ·Neuroguard IEP 3-in-1 Carotid Stent and Post-Dilation Balloon System with Integrated Embolic Protection

    Stent, Carotid

    FDA Pre-Market Approval
    FDA Class 3 ·Neuroguard IEP® 3-in-1 Carotid Stent, Post-Dilatation Balloon System with Integrated Embolic Protection

    Stent, Carotid

    FDA Pre-Market Approval
    FDA Class 3 ·Neuroguard IEP® 3-in-1 Carotid Stent, Post-Dilation Balloon System with Integrated Embolic Protection

    MaXcess

    FDA UDI
    Nuvasive, Inc.·00887517431905·MaXcess 4 Inserter, Low Profile Shim

    MIRABAY

    FDA UDI
    Mirabay Orthodontics Corp.·05065025111488·CRIMPABLE STOPS SMALL STAINLESS 0.012-0.018 PK100

    ANTI-ROTATION SLEEVE

    FDA UDI
    Osteocentric Technologies, Inc.·00810189110373·ANTI-ROTATION SLEEVE

    M/DN®

    FDA UDI
    Zimmer, Inc.·00889024040090·

    M/DN®

    FDA UDI
    Zimmer, Inc.·00889024040076·

    M/DN®

    FDA UDI
    Zimmer, Inc.·00889024040083·

    Plateau-X Spacer System

    FDA UDI
    Life Spine, Inc.·00190837012458·

    iQFlex Pro

    FDA 510(k)
    FDA Class 2 ·Radiology

    PROCLAIM¿ DRG IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code PMP·August 5, 2019

    M/DN®

    FDA UDI
    Zimmer, Inc.·00889024040212·

    M/DN®

    FDA UDI
    Zimmer, Inc.·00889024040229·

    M/DN®

    FDA UDI
    Zimmer, Inc.·00889024040137·