26 results
·
17ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·MICRO STENT II OVER-THE-WIRE CORONARY STENT SYSTEM
Ventilator, High Frequency
FDA Pre-Market Approval
FDA Class 3
·LIFE PULSE HIGH FREQUENCY JET VENTILATOR
Ventilator, High Frequency
FDA Pre-Market Approval
FDA Class 3
·LIFE PULSE HIGH FREQUENCY JET VENTILATOR
Ventilator, High Frequency
FDA Pre-Market Approval
FDA Class 3
·LIFE PULSE HIGH FREQUENCY VENTILATOR ENDOTRACHEAL TUBE ADAPTER
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·Siello T 53; Siello T 60; Siello JT 45; Siello JT 53; Solia T 53; Solia T 60; Solia JT 45; Solia JT 53
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·Siello T 53; Siello T 60; Siello JT 45; Siello JT 53; Solia T 53; Solia T 60; Solia JT 45; Solia JT 53
Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)
FDA Pre-Market Approval
FDA Class 3
·Siello T 53; Siello T 60; Siello JT 45; Siello JT 53; Solia T 53; Solia T 60; Solia JT 45; Solia JT 53
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·Siello T 53, Siello T 60, Siello JT 45, Siello JT 53, Solia T 53, Solia T 60, Solia JT 45, Solia JT 53, Siello S 45, Sie
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·SELOX ST/JT, SETROX S & DEXTRUS
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·DEXTRUS, SELOX ST/JT, SETROX S, AND TILDA T/JT/R STEROID-ELUTING PACING LEADS; SOLOX SLX -BP PACING LEAD
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·Solia S 45, Solia S 53, Solia S 60, Solia JT 45, Solia JT 53, Solia T 53, Solia T 60
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·SELOX ST/JT STEROID-ELUTING PASSIVE-FIXATION ENDOCARDIAL PACKING LEAD MODELS SELOX ST 53, SELOX ST 60, SELOX JT 45 & 53
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·SELOX ST 53,SELOX ST 60,SELOX JT 45,SELOX JT 53,SETROX S 45,SETROX S53,SETROX S60,DEXTRUS 4135,DEXTRUS 4136,DETRUS 4137,
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·Siello T/JT, Solia T/JT, Siello S, Solia S, Evia DR, Evia DR-T, Evia SR, Entovis DR, Entovis DR-T, Entovis SR, Entovis S
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·Selox ST/JT; Siello S; Setrox S, Solia S, Safio S
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·SELOX SR/ST/JT, SETROX S, AND DEXTRUS STEROID-ELUTING LEADS
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·SELOX ST, SELOX JT, SETROX S, DEXTRUS, TILDA, SOLOX SLX, SAFIO
Aortic Valve, Prosthesis, Percutaneously Delivered
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC COREVALVE SYSTEM
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·Setrox S 53; Safio S 53; Dextrus 4136;TILDA R53;Solia S 45/53/60, JT 45/53; Siello S53/60/45/53/60/,JT 45/53;
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·Siello S 45/53/60, Solia S 45/53/60, Siello T 53/60, Siello JT 45/53, Solia T 53/60, Solia JT 45/53, EFH-6F-W