1,108 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·NUCLEUS 24 COCHLEAR IMPLANT SYSTEM
Implant, Auditory Brainstem
FDA Pre-Market Approval
FDA Class 3
·NUCLEUS AUDITORY BRAINSTEM IMPLANT
Cochlear Implant With Combined Electrical Stimulation And Acoustic Amplification
FDA Pre-Market Approval
FDA Class 3
·NUCLEUS HYBRID L24 IMPLANT SYSTEM
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·Cochlear Nucleus® CI522 cochlear implant with Slim Straight electrode, Cochlear Nucleus® CI532 cochlear implant with S
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 COCHLEAR IMPLANT SYSTEM
Device, Angioplasty, Laser, Coronary
FDA Pre-Market Approval
FDA Class 3
·CVX-300-P Excimer Laser System
Glenoid Fossa Prosthesis
FDA Pre-Market Approval
FDA Class 3
·TMJ FOSSA-EMINENCE PROSTHESIS SYSTEM
Cochlear Implant With Combined Electrical Stimulation And Acoustic Amplification
FDA Pre-Market Approval
FDA Class 3
·NUCLEUS 24 HYBRID SYSTEM
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·Nucleus 24 Cochlear Implant System
Device, Angioplasty, Laser, Coronary
FDA Pre-Market Approval
FDA Class 3
·EXCIMER LASER CORONARY ATHERECTOMY (ELCA) CATHETER
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 COCHLEAR IMPLANT SYSTEM- ADULTS
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·NUCLEUS 24 COCHLEAR IMPLANT SYSTEM
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·Nucleus 24 Cochlear Implant System
Device, Removal, Pacemaker Electrode, Percutaneous
FDA Pre-Market Approval
FDA Class 3
·SLS ll/GlideLight Catheters
Normothermic Preservation System For Transplantation Of Initially Unacceptable Donor Lungs
FDA Pre-Market Approval
FDA Class 3
·XVIVO Perfusion System with STEEN Solution Perfusate
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM
Device, Angioplasty, Laser, Coronary
FDA Pre-Market Approval
FDA Class 3
·VITESSE POINT 9 MM X80 & EXTREME POINT 9MM X80 PERCUTANEOUS CORONARY ANGIOPLASTY CATHETER, MODELS 110-004 AND 110-002
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CORDIS SEQUICOR THETA MODELS 233D & 233E