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)