BEUDAMED
    10,000 results · 47ms · Sources: EU EUDAMED, US FDA

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    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VENTAK(R) PRX (TM) II AICD SYSTEM

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VENTAK(R) PRX (TM) II AICD SYSTEM

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VENTAK(R) PRX(R) AICD(TM) SYSTEM

    Renuvion APR Handpiece

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Renuvion/J-Plasma Precise Handpiece

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Renuvion Dermal Handpiece, Renuvion Dermal System

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    J-Plasma Precise FLEX Handpiece

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Stent, Superficial Femoral Artery, Drug-Eluting

    FDA Pre-Market Approval
    FDA Class 3 ·Zilver® PTX® Peripheral Drug- Eluting Stent

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VENTAK PRX AND VENTAK. MINI AUTOMATIC IMPLANTABLE CARDIOVERTER

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VENTAK(R) PRX (TM) MODEL 1700,1705 PULSE GENERATOR

    Stent, Superficial Femoral Artery, Drug-Eluting

    FDA Pre-Market Approval
    FDA Class 3 ·Zilver® PTX® Drug-Eluting Peripheral Stent

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VENTAK(R) PRX (TM) MODEL 1700,1705 PULSE GENERATOR

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VENTAK PRX AND VENTAK MINI AUTOMATIC IMPLANTABLE CARDIOVERTER

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VENTAK(R) PRX (TM) MODEL 1700,1705 PULSE GENERATOR

    Stent, Superficial Femoral Artery, Drug-Eluting

    FDA Pre-Market Approval
    FDA Class 3 ·Zilver® PTX® Peripheral Drug-Eluting Stent

    Stent, Superficial Femoral Artery, Drug-Eluting

    FDA Pre-Market Approval
    FDA Class 3 ·Zilver® PTX® Drug-Eluting Peripheral Stent

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·Ventak(R) PRX (TM) Model 1700,1705 Pulse Generator

    Stent, Superficial Femoral Artery, Drug-Eluting

    FDA Pre-Market Approval
    FDA Class 3 ·Zilver® PTX® Peripheral Drug-Eluting Stent

    Stent, Superficial Femoral Artery, Drug-Eluting

    FDA Pre-Market Approval
    FDA Class 3 ·Zilver® PTX® Drug-Eluting Peripheral Stent

    Bone Sonometer

    FDA Pre-Market Approval
    FDA Class 2 ·ACHILLES EXPRESS ULTRASONOMETER