10,000 results · 377ms · Sources: EU EUDAMED, US FDA

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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