1,979 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MAESTRO SERIES 500 P.G. MODELS 501, 505, 509
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MAESTRO SERIES 500 P.G.& MODEL 1006 PACEMAKER PROG
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MAESTRO(R) II MODEL 533 PACEMAKER SYSTEM
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MAESTRO SERIES 500 P.G.& MODEL 1006 PACEMAKER PROG
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MAESTRO(R) II MODEL 533 PACEMAKER SYSTEM
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·MASTRO SAVVI SERIES 300 VDD PACING SYSTEM
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·CCS MODEL 300 PACEMAKER MAESTRO
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·MAESTRO(R) SAVVI(TM) SERIES 300 VDD PACING SYSTEM
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·POLYSAFE(TM) A-TRACK(TM) MODEL AT-332 ENDOCARDIAL
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MAESTRO SERIES 500 P.G. MODELS 501, 505, 509
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·MAESTRO(R) SAVVI(TM) SERIES 305 VDD PACING SYSTEM
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MAESTRO SERIES 500 P.G. MODELS 501, 505, 509
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·CCS MODEL 333 PACEMAKER SYSTEM
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·MAESTRO(R) SAVVI(TM) SERIES 300 VDD PACING SYSTEM
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·MAESTRO(R) MODEL 1006P PACEMAKER PROGRAMMER
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MAESTRO SERIES 500 P.G.& MODEL 1006 PACEMAKER PROG
Filler, Bone Void, Synthetic Peptide
FDA Pre-Market Approval
FDA Class 3
·i-FACTOR Peptide Enhanced Bone Graft
Coronary Drug-Eluting Stent
FDA Pre-Market Approval
FDA Class 3
·SYNERGY XD Everolimus Eluting Platinum Chromium Coronary Stent System and SYNERGY SHIELD Everolimus Eluting Platinum Chr
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·SCULPTRA AESTHETIC (INJECTABLE POLY-L-LACTIC ACID)
System, Endovascular Graft, Aortic Aneurysm Treatment
FDA Pre-Market Approval
FDA Class 3
·Zenith Dissection Endovascular System