208 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·SICD Gen 2, SICD MRI
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·SICD Gen 2, SICD MRI
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·Gen V CryoConsole RoHS Compliant
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·SICD Gen 2, SICD MRI
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·SICD Gen 2, SICD MRI
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·SICD Gen 2, SICD MRI
Fluid, Intraocular
FDA Pre-Market Approval
FDA Class 3
·Silikon 1000
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MODEL 7271 GEM DR, MODEL 7273 GEM II DR, MODEL 7275 GEM III DR ICDS
Kit, Dna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·CERVISTA HPV 16/18 TEST
Kit, Dna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·CERVISTA HPV HR TEST
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·SICD Gen 2 and SICD MRI
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·Clareon Intraocular Lenses with the AutonoMe Delivery System
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·SICD Gen 2 A209, SICD MRI A219
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·A209 SICD Gen 2, A219 SICD MRI
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·MODELS 7070,7071,7071M,SYNERGEST(TM)II PULSE GEN
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·A209 SICD Gen 2, A219 SICD MRI
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·A209 SICD Gen 2, A219 SICD MRI
Implanted Phrenic Nerve Stimulator For Central Sleep Apnea
FDA Pre-Market Approval
FDA Class 3
·remede System IPG
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·9600 NETWORK PROGRAMMER & X92 PULSE GEN. MODELS
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·S-ICD GEN 2, S-ICD EMBLEM MRI