143 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Stimulator, Low Electric Field, Tumor Treatment
FDA Pre-Market Approval
FDA Class 3
·Optune
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·7F Freezor Cardiac Cryoablation Catheter, 7F Freezor Xtra Cardiac Cryoablation Catheter
Ventricular (Assist) Bypass
FDA Pre-Market Approval
FDA Class 3
·HeartMate 3 Left Ventricular Assist System
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·9F Freezor MAX Cardiac Cryoablation Catheter
Artificial Iris
FDA Pre-Market Approval
FDA Class 3
·CustomFlex Artificial Iris
Artificial Iris
FDA Pre-Market Approval
FDA Class 3
·CustomFlex ArtificialIris
Artificial Iris
FDA Pre-Market Approval
FDA Class 3
·CustomFlex Artificial Iris
Artificial Iris
FDA Pre-Market Approval
FDA Class 3
·CustomFlex Artificial Iris
Agent, Absorbable Hemostatic, Collagen Based
FDA Pre-Market Approval
FDA Class 3
·FUSION MATRIX-DRY
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·HeartStart FR3 Defibrillator
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·HeartStart FR3 Defibrillator
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·HeartStart FR3 Defibrillator
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·HeartStart FR3 Defibrillator
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·Philips HeartStart FR3 Defibrillator
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·Philips HeartStart FR3 Defibrillator
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·HeartStart FR3 Primary Battery (989803150161)
Agent, Absorbable Hemostatic, Collagen Based
FDA Pre-Market Approval
FDA Class 3
·FLOSEAL MATRIX(R)/PROCEED(R) HEMOSTATIC SEALANTS (DRY FORM)
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC MODEL 6725 PIN-PLUG FOR IS-1 PORT
Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)
FDA Pre-Market Approval
FDA Class 3
·Level VIII Controlled Environment Area (CEA), Level IX CEA Dry Room
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Level VIII Controlled Environment Area (CEA), Level IX CEA Dry Room