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 ·SYNERGY™XD 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