18 results
·
44ms
·
Sources: EU EUDAMED, US FDA
DORNIER MEDTECH AMERICA, INC.
FDA registration
DORNIER MEDTECH AMERICA, INC.·1 product·🇺🇸 United States
Hoover Negative Pressure Access Sheath(IVX-NS-1040, IVX-NS-1050, IVX-NS-1140, IVX-NS-1150, IVX-NS-1240, IVX-NS-1250)
FDA registration
INNOVEX MEDICAL CO., LTD.·1 product·🇨🇳 China
Ureteral Access Sheaths (IVX-NS-1040, IVX-NS-1050, IVX-NS-1140, IVX-NS-1150, IVX-NS-1240, IVX-NS-1250)
FDA registration
ETERNAL (SHANGHAI) MEDICAL TECHNOLOGY CO., LTD.·1 product·🇨🇳 China
ADVANCED MEDTECH CORPORATE PTE LTD
FDA registration
ADVANCED MEDTECH CORPORATE PTE LTD·1 product·🇸🇬 Singapore
Hoover Negative Pressure Access Sheath (Hoover) (Hoover Model #'s IVX-NS-1040, IVX-NS-1050, IVX-NS-1140, IVX-NS-1150, IVX-NS-1240, IVX-NS-1250
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Endoscopic Access Overtube, Gastroenterology-Urology
FDA classification
FDA Class 2
·Endoscopic Access Overtube, Gastroenterology-Urology
EzDent-i / E2 / Prora View/ Smart M Viewer
FDA registration
Ewoosoft Co., Ltd·1 product·🇰🇷 South Korea
Fogarty Arterial Embolectomy Catheter with Gate Valve
FDA registration
EDWARDS LIFESCIENCES TECHNOLOGY SARL·1 product·🇺🇸 United States
Fogarty Arterial Embolectomy Catheter with Gate Valve
FDA registration
EDWARDS LIFESCIENCES LLC·1 product·🇺🇸 United States
Fogarty Arterial Embolectomy Catheter with Gate Valve
FDA registration
BECTON, DICKINSON AND COMPANY·1 product·🇺🇸 United States
Atricure2121 (GR,LN*,LS*) - AtriClip PRO-Mini LAA Exclusion System (PROM)
FDA registration
ISOMEDIX OPERATIONS INC·1 product·🇺🇸 United States
Atricure2121 (GR,LN*,LS*) - AtriClip PRO-Mini LAA Exclusion System (PROM)
FDA registration
Isomedix Operations, Inc.·1 product·🇺🇸 United States
Atricure2121 (GR,LN*,LS*) - AtriClip PRO-Mini LAA Exclusion System (PROM)
FDA registration
Isomedix Operations, Inc.·1 product·🇺🇸 United States
BioFire Warrior Panel Control Kit
FDA registration
BioFire Defense, LLC·2 products·🇺🇸 United States
BALTEUM - ONE Lumbar Plate System
FDA 510(k)
FDA Class 2
·Orthopedic
ASPIVIX v1.1 Cervical Suction Tenaculum
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Tenaculum, Uterine
FDA classification
FDA Class 2
·Tenaculum, Uterine
Appliance, Fixation, Spinal Intervertebral Body
FDA classification
FDA Class 2
·Appliance, Fixation, Spinal Intervertebral Body