BEUDAMED
    1,099 results · 20ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 3 ×

    Device, Removal, Pacemaker Electrode, Percutaneous

    FDA Pre-Market Approval
    FDA Class 3 ·SPECTRANETICS LASER SHEATH DEVICE

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·CORDIS SEQUICOR THETA MODELS 233D & 233E

    Implant, Cochlear

    FDA Pre-Market Approval
    FDA Class 3 ·NUCLEUS MULTICHANNEL IMPLANTABLE HEARING PROSTHESI

    Device, Removal, Pacemaker Electrode, Percutaneous

    FDA Pre-Market Approval
    FDA Class 3 ·SPECTRANETICS LASER CATHETERS SLS II LASER SHEATH

    Device, Angioplasty, Laser, Coronary

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

    Oximeter, Fetal Pulse

    FDA Pre-Market Approval
    FDA Class 3 ·OXIFIRST FETAL OXYGEN SATURATION MONITORING SYSTEM

    Implant, Cochlear

    FDA Pre-Market Approval
    FDA Class 3 ·MINI SPEECH PROCESSOR

    Normothermic Preservation System For Transplantation Of Initially Unacceptable Donor Lungs

    FDA Pre-Market Approval
    FDA Class 3 ·XPS™ with Steen Solution™ Perfusate

    Prosthesis, Intervertebral Disc

    FDA Pre-Market Approval
    FDA Class 3 ·MOBI-C CERVICAL DISC PROSTHESIS

    Oximeter, Fetal Pulse

    FDA Pre-Market Approval
    FDA Class 3 ·OXIFIRST FETAL OXYGEN SATURATION MONITORING SYSTEM

    Device, Angioplasty, Laser, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·ELCA Laser Catheters

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·CORDIS SEQUICOR THETA MODELS 233D & 233E

    Device, Angioplasty, Laser, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·CVX-300 Excimer Laser System and ELCA Coronary Atherectomy Catheters

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·CORDIS SEQUICOR THETA MODELS 233D & 233E

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·CORDIS SEQUICOR THETA MODELS 233D & 233E

    Implant, Cochlear

    FDA Pre-Market Approval
    FDA Class 3 ·NUCLEUS MULTICHANNEL IMPLANTABLE HEARING PROSTHESI

    Implant, Cochlear

    FDA Pre-Market Approval
    FDA Class 3 ·NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM

    Implant, Cochlear

    FDA Pre-Market Approval
    FDA Class 3 ·NUCLEUS 24 CONTOUR COCHLEAR IMPLANT SYSTEM

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·CORDIS SEQUICOR THETA MODELS 233D & 233E

    Device, Angioplasty, Laser, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·VITESSE TM -E (ECCENTRIC MONORAIL) CATHETER MODEL 120-008