770 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·VITATRON DA+ C & T SERIES IPGS
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·DEMA IPGS/C & T SERIES IPGS
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·DEMA IPG/C & T SERIES IPGS
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·DEMA IPG/C & T SERIES IPGS
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·DEMA IPG/C & T SERIES IPGS
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·C & T SERIES IPG & DEMA FAMILIES
Pump, Infusion, Implanted, Programmable
FDA Pre-Market Approval
FDA Class 3
·ASCENDA INTRATHECAL CATHETER WITH 86 CM SPINAL SEGMENT, 66CM SPINAL SEGMENT, 86 CM SPINAL SEGMENT REVISION KIT, ACCESSOR
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·DIVA FAMILY, SELECTION AFM C-SERIES AND T-SERIES DEVICES
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·SPRINT QUATTRO LEAD, SPLITTER/ADAPTOR, DF-4 IMPLANT TOOL KIT FOR MDT LEADS
Prosthesis, Ankle, Uncemented, Non-Constrained
FDA Pre-Market Approval
FDA Class 3
·Hintermann Series H3 Total Ankle Replacement System
Prosthesis, Ankle, Uncemented, Non-Constrained
FDA Pre-Market Approval
FDA Class 3
·Hintermann Series H3 Total Ankle Replacement System
Prosthesis, Ankle, Uncemented, Non-Constrained
FDA Pre-Market Approval
FDA Class 3
·Hintermann Series H3 Total Ankle Replacement System
Prosthesis, Ankle, Uncemented, Non-Constrained
FDA Pre-Market Approval
FDA Class 3
·Hintermann Series H3 Total Ankle Replacement System
Prosthesis, Ankle, Uncemented, Non-Constrained
FDA Pre-Market Approval
FDA Class 3
·Hintermann Series H3 Total Ankle Replacement System
Prosthesis, Ankle, Uncemented, Non-Constrained
FDA Pre-Market Approval
FDA Class 3
·Hintermann Series H3 Total Ankle Replacement System
Heart-Valve, Non-Allograft Tissue
FDA Pre-Market Approval
FDA Class 3
·Edwards Pericardial Aortic Bioprosthesis, INSPIRIS RESILIA Aortic Valve, Edwards Pericardial Mitral Bioprosthesis, and t
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·VISTA 4, 6, & T; DELTA T & TRS; VISTA DD; AND VIGOR DDD
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·DIVA IPG FAMILY, DEMA IPG FAMILY, & VARIOUS C-SERIES & T-SERIES DEVICES
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·DEMA FAMILIES & DIVA FAMILIES & SELECTION AFM & C-SERIES & T- SERIES
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·KRONOS LV-T CRT-D & LUMAX VR/DR/HF (-T) ICDS & CDT-DS