576 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·PSW 1803.U / HMSC 3.40.2 / CardioMessenger Smart
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
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·PSW 1803.U / HMSC 3.40.2 /CardioMessenger Smart
Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)
FDA Pre-Market Approval
FDA Class 3
·PSW 1803.U /HMSC 3.40.2 / CardioMessenger Smart
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·Defibrillator, Implantable, Dual Chamber, Automatic Implantable Cardioverter with Cardiac Resynchronization
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·Pulse Generator, Permanent Implantable
Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)
FDA Pre-Market Approval
FDA Class 3
·Pulse Generator, Pacemaker, Implantable with Cardiac Resynchronization (CRT_P)
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·Pacemaker ICD CRT Non Implanted components.
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·BELOS, LEXOS, LUMOS, and XELOS
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·PSW 1802.U, ACTROS, AXOS, BA03, CYLOS, DROMOS, KAIROS, PHILOS, PHILOS II, PROTOS, EVIA, ENTOVIS, ECURO, EFFECTA, ESTELLA
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
·IFORIA 5/7, ILESTO 57/, INVENTRA 7, IPERIA 5/7, ITREVIA 5/7, ILIVIA 5/7, INTICA 5/7, INLEXA 5/7, LUMAX 300/340 and 500/5
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
·STRATOS, EVIA, ENTOIVS, ELUNA 8, EPYRA 8, and ETRINSA 8
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
·Edora 8, Evity 8, Enitra 8, Enticos 8 HF-T QPs,Edora 8, Evity 8, Enitra 8, Enticos 8 HF-Ts and PSW 1601.U Pacemaker/ICD/
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·PSW 1601.U Pacemaker/ICD/CRT non implanted components