17 results
·
56ms
·
Sources: EU EUDAMED, US FDA
The Portable ANSiScope
FDA registration
DyAnsys India Private Limited·1 product·🇮🇳 India
THE PORTABLE ANSISCOPE
FDA 510(k)
FDA Class 2
·Cardiovascular
Synergy Health AST, LLC
FDA registration
Synergy Health AST, LLC·1 product·🇺🇸 United States
NeuraGen Nerve Guide
FDA registration
Sterigenics U.S., LLC·1 product·🇺🇸 United States
NeuraGen Nerve Guide
FDA registration
INTEGRA LIFESCIENCES CORPORATION·1 product·🇺🇸 United States
NeuraGen Nerve Guide
FDA registration
INTEGRA NEUROSCIENCES·1 product·🇺🇸 United States
Synergy Health AST, LLC
FDA registration
Synergy Health AST, LLC·1 product·🇺🇸 United States
ALLOMATRIX
FDA registration
WRIGHT MEDICAL TECHNOLOGY, INC.·1 product·🇺🇸 United States
NeuraGen Nerve Guide
FDA registration
Integra LifeSciences Corporation·1 product·🇺🇸 United States
NeuraGen Nerve Guide
FDA registration
Integra LifeSciences Corporation·1 product·🇺🇸 United States
D187816
FDA registration
STERITECH, INC.·1 product·🇺🇸 United States
ALLOMATRIX
FDA registration
WRIGHT MEDICAL TECHNOLOGY, INC.·1 product·🇺🇸 United States
NEUROGEN NERVE GUIDE
FDA 510(k)
FDA Class 2
·Neurology
JUMP START, MODEL 970300
FDA 510(k)
FDA Class 3
·Cardiovascular
Electrocardiograph
FDA classification
FDA Class 2
·Electrocardiograph
Cuff, Nerve
FDA classification
FDA Class 2
·Cuff, Nerve
Automated External Defibrillators (Non-Wearable)
FDA classification
FDA Class 3
·Automated External Defibrillators (Non-Wearable)