BEUDAMED
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    APYX-044-BPS Renuvion/J-Plasma Precise Open 44mm, a.k.a BVX-044-BPS Renuvion/J-Plasma Precise Open 44mm

    FDA registration
    Apyx Medical Corporation·1 product·🇺🇸 United States

    Device, Removal, Pacemaker Electrode, Percutaneous

    FDA Pre-Market Approval
    FDA Class 3 ·CVX-300 EXCIMER LASER VERSION V3.7.12/V3.8.12

    Device, Angioplasty, Laser, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·CVX-300 EXCIMER LASER VERSION V3.7.12/V3.8.12

    Device, Angioplasty, Laser, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·SPECTRANETICS EXCIMER LASER

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756593991·PAD 1.26 X .55 (VAS. SOL.)

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756826167·PAD 1 in ROUND (VAS. SOL.)

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756593229·MED MULTI PURPOSE TUBE HOLDER

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756593908·Hemostatic Pad 1.75x1.10 Rev E

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VENTAK PRX, VENTAK MINI

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VENTAK PRX AICD SYSTEM

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VENTAK PRX/MINI FAMILIES

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VENTAK PRX AICD SYSTEM

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VENTAK PRX AICD SYSTEM

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VENTAK PRX AICD SYSTEM

    Device, Angioplasty, Laser, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·CVX-300 LASER SYSTEM

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VENTAK PRX AICD SYSTEM

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VENTAK PRX, VENTAK MINI

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VENTAK PRX,VENTAK MINI

    Implantable Pacemaker Pulse-Generator

    FDA Pre-Market Approval
    FDA Class 3 ·TRILOGY SR+ MODEL 2260L & 2264L CARDIAC PULSE GENERATORS WITH THE MODEL 3023 PDX FUNCTION PACK

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VENTAK PRX AICD, VENTAK PRX II AICD, VENTAK PRX III AICD, VENTAK MINI AICD, VENTAK MINI HC AICD, VENTAK II AICD