Tabla De Contenido; Introduction - Stryker System 6 Manual Del Usuario

EN
Contents
Introduction .................................................................2
Indications For Use .....................................................3
Contraindications ........................................................3
For Use With ...............................................................3
User/Patient Safety .....................................................4
Definitions ...................................................................4
Instructions ..................................................................5
To Install Non-sterile Battery .................................5
Sterile Assistant Action .....................................5
Circulating Assistant Action...............................6
Sterile Assistant Action .....................................6
To Replace Battery ................................................7
Care Instructions .........................................................7
Specifications .............................................................7
2

Introduction

This Instructions For Use manual is the most
comprehensive source of information for the safe
and effective use of your product. This manual may
be used by in-service trainers, physicians, nurses,
surgical technologists, and biomedical equipment
technicians. Keep and consult this reference manual
during the life of the product.
The following conventions are used in this manual:
• A WARNING highlights a safety-related issue.
ALWAYS comply with this information to prevent
patient and/or healthcare staff injury.
• A CAUTION highlights a product reliability issue.
ALWAYS comply with this information to prevent
product damage.
• A NOTE supplements and/or clarifies procedural
information.
If additional information or in-service training is
required, contact your Stryker sales representative
or call Stryker customer service. Outside the US,
contact your nearest Stryker subsidiary.
NOTE: The user and/or patient should report
any serious product-related incident to both the
manufacturer and the Competent Authority of the
European Member State where the user and/or
patient is established.
6126-120-700 Rev-AA
www.stryker.com