1,299 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Glenoid Fossa Prosthesis
FDA Pre-Market Approval
FDA Class 3
·TMJ FOSSA-EMINENCE PROSTHESIS SYSTEM
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·Nucleus® 22 Cochlear Implant System
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CORDIS SEQUICOR THETA MODELS 233D & 233E
Device, Removal, Pacemaker Electrode, Percutaneous
FDA Pre-Market Approval
FDA Class 3
·Spectranetics Laser Sheath (SLS) II and GlideLight Laser Sheath
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM
Glenoid Fossa Prosthesis
FDA Pre-Market Approval
FDA Class 3
·TMJ FOSSA EMINENCE/CONDYLAR PROSTHESIS SYSTEM
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·NUCLEUS 24 COCHLEAR IMPLANT SYSTEM (CI24R & CI24RE MODELS)
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·NUCLEUS 24 COCHLEAR IMPLANT SYSTEM
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·COCHLEAR IMPLANT SYSTEM
Device, Removal, Pacemaker Electrode, Percutaneous
FDA Pre-Market Approval
FDA Class 3
·SPECTRANETICS LASER SHEATH II PRODUCTS
Implant, Auditory Brainstem
FDA Pre-Market Approval
FDA Class 3
·Nucleus Auditory Brainstem Implant System
Implant, Auditory Brainstem
FDA Pre-Market Approval
FDA Class 3
·Nucleus 24 Auditory Brainstem Implant
Implant, Auditory Brainstem
FDA Pre-Market Approval
FDA Class 3
·Nucleus Auditory Brainstem Implant System
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·Nucleus Cochlear Implant System
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·GEMINI(R) THETA MODEL 415A CARDIAC PACER
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM
Device, Removal, Pacemaker Electrode, Percutaneous
FDA Pre-Market Approval
FDA Class 3
·SPECTRANETICS LASER SHEATHS
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
·Spectranetics Laser Sheath (SLS)
Device, Removal, Pacemaker Electrode, Percutaneous
FDA Pre-Market Approval
FDA Class 3
·SPECTRANTICS SLS II LASER SHEATH