BEUDAMED
    5,264 results · 42ms · Sources: EU EUDAMED, US FDA

    Acid, Hyaluronic, Intraarticular

    FDA Pre-Market Approval
    FDA Class 3 ·SUPARTZ FX and VISCO-3

    Acid, Hyaluronic, Intraarticular

    FDA Pre-Market Approval
    FDA Class 3 ·SUPARTZ FX & VISCO-3

    Acid, Hyaluronic, Intraarticular

    FDA Pre-Market Approval
    FDA Class 3 ·SUPARTZ FX and VISCO-3

    Acid, Hyaluronic, Intraarticular

    FDA Pre-Market Approval
    FDA Class 3 ·Supartz FX and Visco-3

    Aortic Valve, Prosthesis, Percutaneously Delivered

    FDA Pre-Market Approval
    FDA Class 3 ·Medtronic Evolut FX Delivery Catheter System

    Aortic Valve, Prosthesis, Percutaneously Delivered

    FDA Pre-Market Approval
    FDA Class 3 ·Medtronic Evolut FX Delivery Catheter System

    Acid, Hyaluronic, Intraarticular

    FDA Pre-Market Approval
    FDA Class 3 ·SUPARTZ Device Family, Supartz FX, VISCO-3

    Vitreoretinal Cannulae.

    Basic UDI-DI
    EU MDR · Eu Md Class 2a ·Sterimedix Ltd·4 devices

    Aortic Valve, Prosthesis, Percutaneously Delivered

    FDA Pre-Market Approval
    FDA Class 3 ·Medtronic Evolut FX Delivery Catheter and Loading Systems

    Acid, Hyaluronic, Intraarticular

    FDA Pre-Market Approval
    FDA Class 3 ·SUPARTZ device family, SUPARTZ FX and VISCO-3

    Catheters, Transluminal Coronary Angioplasty, Percutaneous

    FDA Pre-Market Approval
    FDA Class 2 ·FX MINIRAIL PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY (PTCA) CATHETER

    Acid, Hyaluronic, Intraarticular

    FDA Pre-Market Approval
    FDA Class 3 ·SUPARTZ device family, SUPARTZ FX and VISCO-3

    Warming drawer unit for infusions

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·FF Fémfeldolgozó Zrt.·1 device

    RETRACTOR

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·FX Shoulder Solutions·1 device

    RASP HOLDER

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·FX Shoulder Solutions·1 device

    Bowl stand with heating

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·FF Fémfeldolgozó Zrt.·1 device

    Catheters, Transluminal Coronary Angioplasty, Percutaneous

    FDA Pre-Market Approval
    FDA Class 2 ·FX MINIRAIL RX PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY (PTCA) CATHETER

    Aortic Valve, Prosthesis, Percutaneously Delivered

    FDA Pre-Market Approval
    FDA Class 3 ·Medtronic Evolut PRO+ System and Medtronic Evolut FX System

    FFX

    Basic UDI-DI
    EU MDD · Eu Md Class 2b ·SC MEDICA·1 device

    FFX

    Basic UDI-DI
    EU MDD · Eu Md Class 2b ·SC MEDICA·1 device