1,138 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Device, Removal, Pacemaker Electrode, Percutaneous
FDA Pre-Market Approval
FDA Class 3
·SLS SPECTRANETICS LASER SHEATHS
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·GEMINI(R) THETA MODEL 415A CARDIAC PACER
Device, Removal, Pacemaker Electrode, Percutaneous
FDA Pre-Market Approval
FDA Class 3
·SPECTRANETICS LASER SHEATH SLS
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
·CVX-300 LASER SYSTEM
Cochlear Implant With Combined Electrical Stimulation And Acoustic Amplification
FDA Pre-Market Approval
FDA Class 3
·Nucleus® Hybrid Implant System
Device, Angioplasty, Laser, Coronary
FDA Pre-Market Approval
FDA Class 3
·SPECTRANECTICS CVX-300 EXCIMER LASER SYSTEM
Joint, Temporomandibular, Implant
FDA Pre-Market Approval
FDA Class 3
·FOSSA-EMINENCE & CONDYLAR PROSTHESIS SYSTEM AND FOSSA-EMINENCE PROSTHESIS SYSTEM
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·NUCLEUS 24 COCHLEAR IMPLANT SYSTEM
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 22 COCHLEAR IMPLANT SYSTEM FOR CHILDREN/ESPRIT 22
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·Nucleus® Cochlear Implant System
Filler, Bone Void, Synthetic Peptide
FDA Pre-Market Approval
FDA Class 3
·i-FACTOR Peptide Enhanced Bone Graft
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·NUCLES 22 CHANNEL COCHLEAR IMPLANT SYSTEM FOR CHIL
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·NUCLEUS 24 AUDITORY BRAINSTEM IMPLANT SYSTEM
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
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
·CORDIS SEQUICOR THETA MODELS 233D & 233E
Device, Angioplasty, Laser, Coronary
FDA Pre-Market Approval
FDA Class 3
·CVX-300 EXCIMER LASER CORONARY ANGIOPLASTY (ELCA) SYSTEM