10,000 results · 83ms · Sources: EU EUDAMED, US FDA

Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

FDA Pre-Market Approval
FDA Class 3 ·EPT-1000 XP CARDIAC ABLATION SYSTEM

Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

FDA Pre-Market Approval
FDA Class 3 ·EPT-1000 XP RF ABLATION SYSTEMS

Cardiac Ablation Percutaneous Catheter

FDA Pre-Market Approval
FDA Class 3 ·EP TECH EPT-1000XP RF ABLATION SYSTEM

Cardiac Ablation Percutaneous Catheter

FDA Pre-Market Approval
FDA Class 3 ·E P TECH EPT-1000 CARDIAC ABLATION SYSTEM

Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

FDA Pre-Market Approval
FDA Class 3 ·EP TECHNOLOGIES EPT-1000 XP RF ABLATION SYSTEM

Cardiac Ablation Percutaneous Catheter

FDA Pre-Market Approval
FDA Class 3 ·E P TECH EPT-1000 CARDIAC ABLATION SYSTEM

Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

FDA Pre-Market Approval
FDA Class 3 ·EP TECHNOLOGIES EPT-1000 XP RF ABLATION SYSTEM

Cardiac Ablation Percutaneous Catheter

FDA Pre-Market Approval
FDA Class 3 ·E P TECH EPT-1000 CARDIAC ABLATION SYSTEM

Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

FDA Pre-Market Approval
FDA Class 3 ·EP TECHNOLOGIES EPT-1000 XP RF ABLATION SYSTEM

Cardiac Ablation Percutaneous Catheter

FDA Pre-Market Approval
FDA Class 3 ·E P TECH EPT-1000 CARDIAC ABLATION SYSTEM

Cardiac Ablation Percutaneous Catheter

FDA Pre-Market Approval
FDA Class 3 ·E P TECH EPT-1000 CARDIAC ABLATION SYSTEM

Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

FDA Pre-Market Approval
FDA Class 3 ·EP TECHNOLOGIES EPT-1000 XP RF ABLATION SYSTEM

EPTE BIPOLAR

Basic UDI-DI
EU MDR · Eu Md Class 2a ·IONCLINICS & DEIONIC, S.L.·2 devices

E-PT

Basic UDI-DI
EU MDD · Eu Md Class 2b ·GE Healthcare Finland Oy·1 device

EPTE SYSTEM

Basic UDI-DI
EU MDR · Eu Md Class 2a ·IONCLINICS & DEIONIC, S.L.·2 devices

CALLISTO eye

FDA registration
CARL ZEISS MEDITEC AG (OBERKOCHEN)·3 products·🇩🇪 Germany

CALLISTO eye

FDA registration
CARL ZEISS MEDITEC AG (Munich)·3 products·🇩🇪 Germany

RECORDER REMOTE CABLE 3P

FDA UDI
OLYMPUS MEDICAL SYSTEMS CORP.·04953170396175·

INFRARED AND BLUE LIGHT FILTER UNIT

FDA UDI
OLYMPUS MEDICAL SYSTEMS CORP.·04953170396113·

Infrared imaging unit

FDA UDI
OLYMPUS MEDICAL SYSTEMS CORP.·04953170424724·