241 results
·
43ms
·
Sources: EU EUDAMED, US FDA
CATHETER, THROMBUS RETRIEVER
FDA registration
NEURAVI LIMITED·1 product·🇮🇪 Ireland
EmboTrap II Revascularization Device
FDA registration
ADVANT MEDICAL LTD·1 product·🇮🇪 Ireland
Synergy Health Ireland Ltd
FDA registration
Synergy Health Ireland Ltd·1 product·🇮🇪 Ireland
EmboTrap ll Revascularization Device
FDA 510(k)
FDA Class 2
·Cardiovascular
Catheter, Thrombus Retriever
FDA classification
FDA Class 2
·Catheter, Thrombus Retriever
L8-18i-RS
FDA registration
GE Healthcare Japan Corporation·3 products·🇯🇵 Japan
GE Logiq P9/P7
FDA registration
NIPPON EVERX K.K.·3 products·🇯🇵 Japan
Salto Talaris Total Ankle Prosthesis
FDA registration
Ascension Orthopedics, Inc.·1 product·🇺🇸 United States
L8-18i-RS
FDA registration
Wipro GE Healthcare Private Ltd.·3 products·🇮🇳 India
L8-18i-RS
FDA registration
GE PARALLEL DESIGN, INC.·3 products·🇺🇸 United States
L8-18i-RS
FDA registration
GE ULTRASOUND KOREA, LTD.·3 products·🇰🇷 South Korea
L8-18i-RS
FDA registration
GE MEDICAL SYSTEMS (CHINA) CO., LTD.·3 products·🇨🇳 China
P8D
FDA registration
HUMANSCAN CO., LTD·3 products·🇰🇷 South Korea
QUALITY TECH SERVICES, LLC
FDA registration
QUALITY TECH SERVICES, LLC·1 product·🇺🇸 United States
L8-18i-RS
FDA registration
PARALLEL DESIGN SAS·3 products·🇫🇷 France
L8-18i-RS
FDA registration
GE Healthcare Austria GmbH & Co OG·3 products·🇦🇹 Austria
Isomedix Operations, Inc.
FDA registration
Isomedix Operations, Inc.·1 product·🇺🇸 United States
MRDx Test
FDA registration
MOLECULARMD CORPORATION·1 product·🇺🇸 United States
MySpine Pedicle Screw Placement Guides MC and Drill Pilot Instruments
FDA registration
BBF STERILISATIONSSERVICE GMBH·1 product·🇩🇪 Germany
ACU-CUT VERTEBRAL AUGMENTATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic