10,000 results
·
45ms
·
Sources: EU EUDAMED, US FDA
OMNI360 Kertomus / version 1.1 (several versions available)
Basic UDI-DI
EU MDD
·
Eu Md Class 1
·CGI Suomi Oy·1 device
Pegasos version 9.2.00 / available in different versions
Basic UDI-DI
EU MDD
·
Eu Md Class 1
·CGI Suomi Oy·1 device
Kemokur 1.5
Basic UDI-DI
EU MDD
·
Eu Md Class 2b
·CGI Suomi Oy·1 device
Merlot Medi Physio 3.0.4
Basic UDI-DI
EU MDD
·
Eu Md Class 2b
·CGI Suomi Oy·1 device
Coronary Drug-Eluting Stent
FDA Pre-Market Approval
FDA Class 3
·SYNERGYXD Everolimus-Eluting Platinum Chromium Coronary Stent System, SYNERGY MEGATRON Everolimus-Eluting Platinum Chr
Sensor, Glucose, Invasive
FDA Pre-Market Approval
FDA Class 3
·PARADIGM REAL-TIME SYSTEM, PARADIGM REAL-TIME REVEL SYSTEM AND GUARDIAN REAL-TIME CGM SYSTEM
JANACEK TUBO-UTERINE IMPLANTATION SET
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Coronary Drug-Eluting Stent
FDA Pre-Market Approval
FDA Class 3
·SYNERGY XD Everolimus Eluting Platinum Chromium Coronary Stent System and SYNERGY SHIELD Everolimus Eluting Platinum Chr
Continuous Glucose Monitor, Implanted, Adjunctive Use
FDA Pre-Market Approval
FDA Class 3
·Eversense E3 Continuous Glucose Monitoring System (CGM System) - Entire System, Eversense E3 Sensor, Eversense E3 Insert
Sensor, Glucose, Implanted, Non-Adjunctive Use
FDA Pre-Market Approval
FDA Class 3
·Eversense E3 Continuous Glucose Monitoring System (CGM System) - Entire System, Eversense E3 Sensor, Eversense E3 Insert
Sensor, Glucose, Implanted, Non-Adjunctive Use
FDA Pre-Market Approval
FDA Class 3
·Eversense E3 Continuous Glucose Monitoring System (CGM System) - Entire System, Eversense E3 Sensor, Eversense E3 Insert
Continuous Glucose Monitor, Implanted, Adjunctive Use
FDA Pre-Market Approval
FDA Class 3
·Eversense E3 Continuous Glucose Monitoring System (CGM System) - Entire System, Eversense E3 Sensor, Eversense E3 Insert
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·USCI(R) PROBE III(TM) BALLOON-ON-A-WIRE(TM) D. SYS
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·USCI(R) PROBE III(TM) BALLOON-ON-A-WIRE(TM) D. SYS
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·USCI(R) PROBE III(TM) BALLOON-ON-A-WIRE(TM) D. SYS
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·USCI(R) PROBE III(TM) BALLOON-ON-A-WIRE(TM) D. SYS
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·USCI PROBE III BALLOON-ON-A-WIRE DILATATION SYSTEM
BOSTON SCIENTIFIC CORPORATION
FDA registration
BOSTON SCIENTIFIC CORPORATION·1 product·🇨🇷 Costa Rica
BOSTON SCIENTIFIC CORPORATION
FDA registration
BOSTON SCIENTIFIC CORPORATION·1 product·🇨🇷 Costa Rica
AbbottVasc (CR1) - ARMADA 35
FDA registration
Synergy Health AST, SRL·2 products·🇨🇷 Costa Rica