4,690 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
·AUTIMA(TM) MODEL 2251 & MODEL 2600
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·REFLEX MODEL 8223E DUAL CHAMBER PULSE GENERATOR
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·AUTIMA(TM) MODEL 2251 & MODEL 2600
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASOSEAL (TM)
Programmer, Pacemaker
FDA Pre-Market Approval
FDA Class 3
·APPLICATION SOFTWARE MODEL 3307 (VERSION 4.1A)
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·LEX MODEL 8220E SINGLE CHAMBER PULSE GENERATOR
Programmer, Pacemaker
FDA Pre-Market Approval
FDA Class 3
·MODEL 3264 REV. B PROGRAMMER SOFTWARE FOR THE APSU MODEL 3250 PROGRAMMER
Programmer, Pacemaker
FDA Pre-Market Approval
FDA Class 3
·V1. 2A PROGRAMMER SOFTWARE
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·META III MODEL 1206,1206E,1206M PACING SYSTEMS
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MODEL 283 PULSE GENERATOR & MODEL 370 PROGRAMMER
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·REGENCY SC+, REGENCY SC, REGENCY SCX
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·PARAGON, PHOENIX, MULTILOG & SENSORITHM PACEMAKERS
Tissue Graft Of 6mm And Greater
FDA Pre-Market Approval
FDA Class 3
·N.C.G.T. GRAFT
Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)
FDA Pre-Market Approval
FDA Class 3
·SENSOLOG/DIALOG/REGENCY FAMILY OF PACEMAKERS
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·X-PRESS 6 FRENCH VASCULAR CLOSURE SYSTEM
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·SENSOLOG MODEL 703 PULSE GENERATOR & P700 PROGRAMM
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·REFLEX MODELS 8218 AND 822OE; REFLEX DDD MODELS 8223E AND 8224; AND SIMPLEX MODEL 8232 PULSE GENERATORS
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·APS III PROGRAMMER WITH SOFTWARE MODEL 3302 REV.D (V1.04)
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·VASOSEAL EXTRA SECURITY (ES) DEVICE
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·SENSOLOG (R) ULTILOG (TM) MODELS 2040K,2040T