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Sistema de neuromodulación sacra, venta exclusiva bajo prescripción médica
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Table of contents
TABLE OF CONTENTS .......................................................................................................................................................................... 5
INTRODUCTION.................................................................................................................................................................................. 6
PURPOSE OF THE TRIAL SYSTEM......................................................................................................................................................... 6
CONTRAINDICATIONS......................................................................................................................................................................... 6
WARNINGS ........................................................................................................................................................................................ 6
PRECAUTIONS.................................................................................................................................................................................... 7
INDIVIDUALIZATION OF TREATMENT ................................................................................................................................................ 11
ADVERSE EVENTS............................................................................................................................................................................. 11
PATIENT COUNSELING INFORMATION ............................................................................................................................................... 11
DEVICE DESCRIPTION....................................................................................................................................................................... 12
SPECIFICATIONS............................................................................................................................................................................... 13
ACTIVATING THE TRIAL STIMULATOR ................................................................................................................................................ 14
CONNECTING THE TRIAL STIMULATOR TO THE TINED LEAD OR PNE LEAD........................................................................................... 15
INSERTING TRIAL STIMULATOR INTO THE BELT................................................................................................................................. 16
REPLACEMENT AND DISPOSAL......................................................................................................................................................... 16
LABEL SYMBOLS.............................................................................................................................................................................. 17
WIRELESS COMMUNICATION............................................................................................................................................................ 18
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