1,087 results
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19ms
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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 22 COCHLEAR IMPLANT SYSTEM- CHILDREN
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·NUCLEUS 24 COCHLEAR IMPLANT SYSTEM
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 24 COCHLEAR IMPLANT SYSTEM
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·Mobi-C Cervical Disc Prosthesis Two Level
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·Mobi-C Cervical Disc Prosthesis (One-Level Indication)
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