103 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Device, Testicular Hypothermia
FDA Pre-Market Approval
FDA Class 3
·REPRO-MED - THD
Pacemaker/Icd/Crt Non-Implanted Components
FDA Pre-Market Approval
FDA Class 3
·PSW 2202.U and NEO 2202.U
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·PSW 2100.U and NEO 2100.U
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·PSW 2100.U and NEO 2100.U
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·PSW 2100.U and NEO 2100.U
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·PSW 2100.U and NEO 2100.U
Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)
FDA Pre-Market Approval
FDA Class 3
·PSW 2100.U and NEO 2100.U
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC IMPLANTABLE CARDIO-VERTER DEFIBRILLATOR SYSTEMS ENTRUST ICOS
Pacemaker/Icd/Crt Non-Implanted Components
FDA Pre-Market Approval
FDA Class 3
·PSW 2201.U/1 and NEO 2201.U/1
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·PSW 2201.U/1 and NEO 2201.U/1
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·PSW 2201.U/1 and NEO 2201.U/1
Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)
FDA Pre-Market Approval
FDA Class 3
·PSW 2201.U/1 and NEO 2201.U/1
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·PSW 2201.U/1 and NEO 2201.U/1
Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)
FDA Pre-Market Approval
FDA Class 3
·Pacemaker/ICD/CRT Non-Implanted Components PSW 2202.U and NEO 2202.U
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·Pacemaker/ICD/CRT Non-Implanted Components PSW 2202.U and NEO 2202.U
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·Pacemaker/ICD/CRT Non-Implanted Components PSW 2202.U and NEO 2202.U
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Ilivia Neo 7 VR-T, Intica Neo 7 VR-T DX, Plexa ProMRI DF-1 S DX 65/17, Plexa ProMRI DF-1 S DX 65/15, Plexa ProMRI S 60,
Stent, Carotid
FDA Pre-Market Approval
FDA Class 3
·Neuroguard IEP® 3-in-1 Carotid Stent, Post-Dilation Balloon System with Integrated Embolic Protection
Stent, Carotid
FDA Pre-Market Approval
FDA Class 3
·Neuroguard IEP® 3-in-1 Carotid Stent, Post-Dilatation Balloon System with Integrated Embolic Protection
Stent, Carotid
FDA Pre-Market Approval
FDA Class 3
·Neuroguard IEP 3-in-1 Carotid Stent and Post-Dilation Balloon System with Integrated Embolic Protection