294 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Permanent Defibrillator Electrodes
FDA Pre-Market Approval
FDA Class 3
·KAINOX VCS,SLX 58/11-BP,SLX 58/13-BP,SLX 58/14-BP,SLX 58/15-BP,SLX 58/17-BP,LINOX S 65,LINOX S 75, LINOX T 65,LINOX T75,
Stent, Iliac
FDA Pre-Market Approval
FDA Class 3
·BARD E-LUMINEXX VASCULAR STENT
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Attain Bipolar OTW Lead and Attain OTW LV Lead
Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·Attain StarFix Lead
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·CapSure VDD-2 Lead and Vitatron Brilliant S+VDD Lead
Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)
FDA Pre-Market Approval
FDA Class 3
·STRATOS LV,EVIA HF,EVIA HF-T,ENTOVIS HF,ENTOVIS HF-T,COROX OTW 85 UP STEROID,COROX OTW 75-BP,COROX OTW 85-BP,COROX OTW-S
Agent, Absorbable Hemostatic, Collagen Based
FDA Pre-Market Approval
FDA Class 3
·FLOSEAL MATRIX HEMOSTATIC SEALANT DEVICE
System, Endovascular Graft, Arteriovenous (Av) Dialysis Access Circuit Stenosis Treatment
FDA Pre-Market Approval
FDA Class 3
·BARD FLAIR ENDOVASCULAR STENT GRAFT
Stent, Superficial Femoral Artery
FDA Pre-Market Approval
FDA Class 3
·BARD LIFESTENT VASCULAR STENT SYSTEMS
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·EVIA DR, EVIA DR-T,EVIA SR, EVIA SR-T,ENTOVIS DR, ENTOVIS DR-T,ENTOVIS SR,ENTOVIS SR-T,ESTELLA SR,ESTELLA SR-T,ECURO DR,
Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker Electrodes
FDA Pre-Market Approval
FDA Class 3
·CapSure SP Novus Lead, CapSure SP Z Lead, CapSure Z Novus Lead and Vitatron Impulse II Lead
Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker Electrodes
FDA Pre-Market Approval
FDA Class 3
·CapSureFix Lead, CapSureFix Novus Lead and Vitatron Crystalline Active Fixation Lead
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·COROX OTW 85 UP STEROID, LUMAX 300 DR-T, LUMAX 340 DR-T,LUMAX 300 VR-T, LUMAX 340 VR-T, LUMAX 500 DR-T,LUMAX 540 DR-T, L
Permanent Defibrillator Electrodes
FDA Pre-Market Approval
FDA Class 3
·HV Splitter/Adaptor kit and Sprint Quattro Lead
Drug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·Attain Ability Lead and Attain Performa Lead
System, Test, Her-2/Neu, Ihc
FDA Pre-Market Approval
FDA Class 3
·Bond Oracle HER2 IHC System
Stimulator, Electrical, Implantable, For Incontinence
FDA Pre-Market Approval
FDA Class 3
·InterStim Therapy System and Verify Evaluation System (SNS Urinary)
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·Restore, Itrel, Synergy and Intellis Spinal Cord Stimulation Systems and Pisces, Specify, and Vectris Spinal Cord Stimul
Heart-Valve, Non-Allograft Tissue
FDA Pre-Market Approval
FDA Class 3
·Trifecta Valve with Glide Technology (Trifecta GT)
Implanted Electrical Device Intended For Treatment Of Fecal Incontinence
FDA Pre-Market Approval
FDA Class 3
·InterStim Therapy System and Verify Evaluation System (SNS Bowel)