153 results
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29ms
·
Sources: EU EUDAMED, US FDA
HEARTLIGHT
FDA Adverse Event
Injury
·CARDIOFOCUS·Product code OAE·November 26, 2018
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·HEARTLIGHT ENDOSCOPIC ABLATION SYSTEM
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·HeartLight Catheter, HeartLight X3 Console V2
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·HeartLight Endoscopic Ablation System
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·HeartLight System
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·HeartLight Endoscopic Ablation System
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·Heart Light Catheter with Excalibur Balloon
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·HeartLight Endoscopic Ablation System
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·HeartLight Catheter, HeartLight X3 Console V2
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·HeartLight System
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·HeartLight X3 Endoscopic Ablation System
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·HeartLight® X3 Catheter with Excalibur Balloon
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·HeartLight Endoscopic Ablation System
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·HeartLight Endoscopic Ablation System
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·HeartLight Catheter and HeartLight Console
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·HeartLight Endoscopic Ablation System
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·HeartLight Endoscopic Ablation System
Oticon
FDA UDI
Oticon A/S·05707131279606·ALTA PRO, DESIGNRITE 10 WL THP
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587P1509260·15mm PLIF Implant 9mm Wide 26mm Length
TMA - Archwire
FDA UDI
ORMCO CORPORATION·00889989029482·TMA REV.CURVE/LOOPS 016X022 40MM PK/5