ECG Cable/Leadwires

FDA registration

SHENZHEN CORERAY TECHNOLOGY CO., LTD.·1 product·🇨🇳 China

ECG Cable/Leadwires

FDA 510(k)

FDA Class 2 ·Cardiovascular

Cable, Transducer And Electrode, Patient, (Including Connector)

FDA classification

FDA Class 2 ·Cable, Transducer And Electrode, Patient, (Including Connector)

GE Probe

FDA registration

Medical Resale PTY Limited·3 products·🇦🇺 Australia

Vivid e

FDA registration

GE PARALLEL DESIGN, INC.·3 products·🇺🇸 United States

GE 8L-RS

FDA registration

Modality Group Ltd·3 products·🇬🇧 United Kingdom

Vivid e

FDA registration

GE Medical Systems Ultrasound & Primary Care Diagnostics LLC·3 products·🇺🇸 United States

POWERFLEX PRO Percutaneous Transluminal Angioplasty Catheter

FDA registration

Nitinol Devices & Components Costa Rica, S. R. L.·1 product·🇨🇷 Costa Rica

Synergy Health AST, SRL

FDA registration

Synergy Health AST, SRL·1 product·🇨🇷 Costa Rica

Vivid e

FDA registration

GE Healthcare Japan Corporation·3 products·🇯🇵 Japan

Logiq e

FDA registration

CANUTE INTERNATIONAL MEDICAL SERVICES (CANADA) INC·3 products·🇨🇦 Canada

Vivid e

FDA registration

PARALLEL DESIGN SAS·3 products·🇫🇷 France

ISOMEDIX OPERATIONS INC

FDA registration

ISOMEDIX OPERATIONS INC·1 product·🇺🇸 United States

VOMARK TECHNOLOGIES INC

FDA registration

VOMARK TECHNOLOGIES INC·3 products·🇺🇸 United States

Vivid e

FDA registration

GE MEDICAL SYSTEMS (CHINA) CO., LTD.·3 products·🇨🇳 China

Powerflex Pro Percutaneous Transluminal Angioplasty Catheter

FDA registration

Cordis US Corp.·1 product·🇺🇸 United States

Guangzhou Telefield Limited

FDA registration

Guangzhou Telefield Limited·2 products·🇨🇳 China

GE LOGIQ I COMAPACT ULTRASOUND, GE LOGIQ E COMPACT ULTRASOUND, GE VIVID E COMPACT ULTRASOUND

FDA 510(k)

FDA Class 2 ·Radiology

POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER

FDA 510(k)

FDA Class 2 ·Cardiovascular

Catheter, Angioplasty, Peripheral, Transluminal

FDA classification

FDA Class 2 ·Catheter, Angioplasty, Peripheral, Transluminal