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