10,000 results
·
37ms
·
Sources: EU EUDAMED, US FDA
Pinnacle
FDA UDI
Harmar Summit, LLC·00817650026188·Chassis W/O OBS-Sensors
Pinnacle
FDA UDI
Harmar Summit, LLC·00817650026225·Chassis Power W/O OBS Sensors
Pinnacle
FDA UDI
Harmar Summit, LLC·00817650026263·Chassis Power W/O OBS Sensors
AGENT Paclitaxel-Coated Balloon Catheter
FDA registration
Boston Scientific Limited·1 product·🇮🇪 Ireland
AGENTTM Paclitaxel-Coated Balloon Catheter
FDA registration
HEMOTEQ·1 product·🇩🇪 Germany
Synergy Health AST, LLC
FDA registration
Synergy Health AST, LLC·1 product·🇺🇸 United States
Synergy Health AST, LLC
FDA registration
Synergy Health AST, LLC·1 product·🇺🇸 United States
AGENT Paclitaxel-Coated Balloon Catheter
FDA registration
Boston Scientific Corp., Marina Bay Cust. Fulfillment Center·1 product·🇺🇸 United States
AGENT Paclitaxel-Coated Balloon Catheter
FDA registration
Boston Scientific Corporation·1 product·🇺🇸 United States
AGENT Paclitaxel-Coated Balloon Catheter
FDA registration
BOSTON SCIENTIFIC CORPORATION·1 product·🇺🇸 United States
SELUTION SLR 014 PTCA BALLOON CATHETER
FDA registration
MEDALLIANCE, LLC·1 product·🇺🇸 United States
Drug-Eluting Percutaneous Transluminal Coronary Angioplasty Catheter
FDA Pre-Market Approval
FDA Class 3
·AGENT Paclitaxel-Coated Balloon Catheter
Drug-Eluting Percutaneous Transluminal Coronary Angioplasty Catheter
FDA Pre-Market Approval
FDA Class 3
·AGENT Paclitaxel-Coated Balloon Catheter
Drug-Eluting Percutaneous Transluminal Coronary Angioplasty Catheter
FDA Pre-Market Approval
FDA Class 3
·AGENT Paclitaxel-Coated Balloon Catheter
Drug-Eluting Percutaneous Transluminal Coronary Angioplasty Catheter
FDA Pre-Market Approval
FDA Class 3
·AGENT Paclitaxel-Coated Balloon Catheter
Drug-Eluting Percutaneous Transluminal Coronary Angioplasty Catheter
FDA Pre-Market Approval
FDA Class 3
·AGENT Paclitaxel-Coated Balloon Catheter
FIRST MEDIC MODE 610
FDA 510(k)
FDA Class 3
·Cardiovascular
CONTINUOUS PASSIVE MOTION PATIENT KIT OR RE. PAD
FDA 510(k)
FDA Class 1
·Physical Medicine
HEARTSTART 2000
FDA 510(k)
FDA Class 3
·Cardiovascular
HEARTSTART 2000, MANUAL DEFIBRILLATOR
FDA 510(k)
FDA Class 2
·Cardiovascular