10,000 results
·
377ms
·
Sources: EU EUDAMED, US FDA
EYEVAN
FDA UDI
EYEVAN INC.·04582667985020·
K-LINK OPTICAL TECHNOLOGY CO., LTD.
Manufacturer
🇨🇳 China
Spatula and packer d.e. #91 5-3/4". S/S
Device
EU MDR
·
Eu Md Class 1
·HB Meditech (Pvt) Limited·On the market
OPKO HEALTH SPAIN S.L.U.
Manufacturer
🇪🇸 Spain·9 Basic UDI-DIs·9 Devices·ISTITUTO SUPERIORE DI SANITA', ISTITUTO SUPERIORE DI SANITA', ISTITUTO SUPERIORE DI SANITA', and ISTITUTO SUPERIORE DI SANITA'
S.A.L.F. S.p.A. Laboratorio Farmacologico
Manufacturer
🇮🇹 Italy·21 Basic UDI-DIs·202 Devices·ISTITUTO SUPERIORE DI SANITA', ISTITUTO SUPERIORE DI SANITA', ISTITUTO SUPERIORE DI SANITA', and ISTITUTO SUPERIORE DI SANITA'
GENERAL TOPICS SRL
Manufacturer
🇮🇹 Italy·38 Basic UDI-DIs·38 Devices·ISTITUTO SUPERIORE DI SANITA', ISTITUTO SUPERIORE DI SANITA', ISTITUTO SUPERIORE DI SANITA', and ISTITUTO SUPERIORE DI SANITA'
Medicap S.r.l
Manufacturer
🇮🇹 Italy·4 Basic UDI-DIs·5 Devices·ISTITUTO SUPERIORE DI SANITA', ISTITUTO SUPERIORE DI SANITA', ISTITUTO SUPERIORE DI SANITA', and ISTITUTO SUPERIORE DI SANITA'
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CareLink SmartSync Viva Consulta Syncra Advisa Ensura Application
Leadless Pacemaker
FDA Pre-Market Approval
FDA Class 3
·CareLink SmartSync Micra VR/AV Application
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·CareLink SmartSync Platform, CareLink SmartSync Host Application, CareLink SmartSync Common Application, CareLink SmartS
Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)
FDA Pre-Market Approval
FDA Class 3
·CareLink SmartSync Viva Consulta Syncra Advisa Ensura Application
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CareLink SmartSync Viva Consulta Syncra Advisa Ensura Application
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·CareLink SmartSync Viva Consulta Syncra Advisa Ensura Application
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·USCI(R) XPRT(TM) BALL. DIL. CATH. W/PRO/PEL(TM)
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·USCI(R) SOLO(TM) BALL. DIL. CATH. W/PRO/PEL COAT
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·USCI(R) FORCE(R) BALL. DIL. CATH. W/PRO/PEL COAT.
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·USCI(R) SPRINT(TM) BALL. DIL. CATH. W/PRO/PEL COAT
OMRON HEALTHCARE Co., Ltd. Matsusaka Factory
FDA registration
OMRON HEALTHCARE Co., Ltd. Matsusaka Factory·1 product·🇯🇵 Japan
OMRON HEALTHCARE Co., Ltd. Matsusaka Factory
FDA registration
OMRON HEALTHCARE Co., Ltd. Matsusaka Factory·4 products·🇯🇵 Japan
SYSTEM CHART SC-1600
FDA registration
FUJIFILM Manufacturing Corp.·1 product·🇯🇵 Japan