Stryker System 6 6212-000-000 Manual Del Usuario página 3

6215-001-700 Rev-AA
User/Patient Safety
WARNINGS:
• Only trained and experienced healthcare professionals
should use this equipment. Before using any system
component or any component compatible with this system,
read and understand the instructions. Pay particular
attention to WARNING information. Become familiar with
the system components prior to use.
• Upon initial receipt and before each use, inspect all
components for damage. Damage may include bent
contacts and cracks in the housing. DO NOT charge or
use if damage is apparent.
• DO NOT use this equipment in areas in which flammable
anesthetics or flammable agents are mixed with air,
oxygen or nitrous oxide.
• DO NOT modify any system component or accessory.
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.
www.stryker.com
Definitions
The symbols located on the equipment and/or labeling are
defined in this section or in the Symbol Definition Chart. See
the Symbol Definition Chart supplied with the equipment.
SYMBOL DEFINITION
General warning sign
To comply with European Community
Batteries Directive 2006/66/EC, this device
has been designed for safe removal of
the batteries at the end-of-life by a waste
Ni-Cd
treatment facility. Infected units should
be decontaminated before they are
sent for recycling. If it is not possible to
decontaminate the unit for recycling, the
hospital should not attempt to remove the
batteries from waste equipment. Continued
disposal of small amounts of portable
batteries to landfill and incineration is
allowed under Directive 2006/66/EC and
Member State regulations.
EN
3