2,568 results
·
17ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Stimulator, Carotid Sinus Nerve
FDA Pre-Market Approval
FDA Class 3
·Barostim NEO System, Barostim NEO2 System
Stimulator, Carotid Sinus Nerve
FDA Pre-Market Approval
FDA Class 3
·BAROSTIM NEO® System
Stimulator, Carotid Sinus Nerve
FDA Pre-Market Approval
FDA Class 3
·BAROSTIM NEO Implantable Pulse Generator (IPG), BAROSTIM NEO Carotid Sinus Lead (CSL) Kit, Programmer System, Carotid Si
Stimulator, Carotid Sinus Nerve
FDA Pre-Market Approval
FDA Class 3
·Barostim System
Stimulator, Carotid Sinus Nerve
FDA Pre-Market Approval
FDA Class 3
·BAROSTIM NEO® System
Stimulator, Carotid Sinus Nerve
FDA Pre-Market Approval
FDA Class 3
·Barostim System
Stimulator, Carotid Sinus Nerve
FDA Pre-Market Approval
FDA Class 3
·Barostim System
Stimulator, Carotid Sinus Nerve
FDA Pre-Market Approval
FDA Class 3
·Barostim NEO Generator, Barostim NEO2 Generator, Barostim Carotid Sinus Lead, Programmer System, Carotid Sinus Lead Repa
Stimulator, Carotid Sinus Nerve
FDA Pre-Market Approval
FDA Class 3
·BAROSTIM NEO® System
Stimulator, Carotid Sinus Nerve
FDA Pre-Market Approval
FDA Class 3
·Barostim System
Stimulator, Carotid Sinus Nerve
FDA Pre-Market Approval
FDA Class 3
·BAROSTIM NEO Implantable Pulse Generator (IPG), BAROSTIM NEO Carotid Sinus Lead (CSL) Kit, Programmer System, Carotid Le
Stimulator, Carotid Sinus Nerve
FDA Pre-Market Approval
FDA Class 3
·Barostim System
Stimulator, Carotid Sinus Nerve
FDA Pre-Market Approval
FDA Class 3
·Barostim System
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·EVERA S D DR ICD, EVERA S VR ICD, EVERA XT DR ICD, EVERA XT VR ICD
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·CLARITY, DIAMOND 3, JADE 3, RUBY 3, TOPAZ 3, VITA 2 DDR, C-SERIES, AND T-SERIES
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MAXIMO II/SECURA/VIRTUOSO II
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·DIVA PLATFORM IMPLANTABLE PULSE GENERATORS AND PRO VIT APPLICATION SOFTWARE VERSION 3.3.2
Immunohistochemistry Test, Dna Mismatch Repair (Mmr) Protein Assay
FDA Pre-Market Approval
FDA Class 3
·VENTANA MMR RxDx Panel
Immunohistochemistry Test, Dna Mismatch Repair (Mmr) Protein Assay
FDA Pre-Market Approval
FDA Class 3
·VENTANA MMR RxDx Panel (Endometrial Cancer with dMMR status)
Immunohistochemistry Test, Dna Mismatch Repair (Mmr) Protein Assay
FDA Pre-Market Approval
FDA Class 3
·VENTANA MMR RxDx Panel (Endometrial Cancer with dMMR status)