Contact Information; Symbol Definitions - Stryker Neptune 2 Instrucciones De Uso

EN
Indications For Use
The Neptune 2 Waste Management
System is intended to be used in the
operating room, pathology, surgical
centers, and doctor's offices to collect
and dispose of surgical fluid waste as
well as collect smoke generated from
electrocautery or laser devices.
Contraindications
The Neptune 2 Waste Management System is
contraindicated against:
▪ Connection directly to chest tubes.
▪ Connection to closed wound drainage
systems.

Contact Information

For additional information, including safety
information, or in-service training, contact your
Stryker sales representative or call Stryker
Neptune Customer Service at 1-800-550-7836.
For Use With
The Stryker Neptune 2 Disposable Manifold
(manifold) for use with the Neptune 2 Waste
Management System, specifically the rover.
Description
The manifold is a non-sterile, disposable device
that provides a fluid path from the suction lines
to the rover canister. The manifold is for single
patient use only. Manifolds with specimen
collection capability have lids that allow the
retrieval of the specimen.

Symbol 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
2
Print Date: Aug 08, 2016 12:02:55 PM
0000012970, Rev. E Effective Date: Aug 8, 2016 11:39:52 AM
SYMBOL
User/Patient Safety
WARNINGS:
▪ 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. Failure
to comply may result in patient and/or
healthcare staff injury.
▪ Only trained and experienced healthcare
professionals should use this equipment.
Failure to comply may result in patient and/
or healthcare staff injury.
▪ Upon initial receipt, inspect each
component for damage. DO NOT use any
equipment if damage is apparent. Failure
to comply may result in patient and/or
healthcare staff injury.
▪ Use only Stryker-approved system
components and accessories, unless
otherwise specified. Failure to comply may
result in patient and/or healthcare staff
injury.
▪ DO NOT disassemble, modify, service, or
repair any system component or accessory,
unless otherwise specified. Call Stryker
Neptune Customer Service.
▪ The manifold is for SINGLE PATIENT USE
ONLY. DO NOT sterilize or reuse. DO NOT
reuse, reprocess, or repackage a single use
device. A single use device is intended for a
single use only. The single use device may
not withstand chemical, chemical vapor, or
high temperature sterilization reprocessing.
Design features may make cleaning
difficult. Reuse may create a serious risk
of contamination and may compromise the
structural integrity of the device resulting
in operational failure. Critical product
information may be lost if the device is
repackaged. Failure to comply may lead
to infection or cross-infection and result in
patient or healthcare staff injury.
SIGN
▪ ALWAYS follow the current local
recommendations and/or regulations
governing environmental protection and the
risks associated with recycling or disposing
of the equipment at the end of its useful
life.
DEFINITION
▪ ALWAYS follow the current local regulations
SINGLE PATIENT
governing biohazard waste to safely handle
USE ONLY
and dispose of surgical waste.
▪ BLOODBORNE PATHOGEN HAZARD
- ALWAYS wear personal protective
equipment (PPE) when operating or
handling this equipment.
- ALWAYS leave tubing attached to the
manifold and close unused ports during
disposal.
- ALWAYS follow local regulations
regarding proper handling and disposal
of biohazard waste.
Failure to comply may cause infection and
result in healthcare staff injury.
Instructions
▪ DO NOT use a manifold that has been
dropped or mishandled (Figure 1). Failure
to comply may cause leakage and result in
patient and/or healthcare staff injury.
▪ DO NOT use a Y-connector to add more
than one suction line to each port
(Figure 2). Failure to comply may cause
cross-contamination and result in patient
injury.
Figure 1 Handle Manifold with Care
Figure 2 One Suction Line Per Port
NOTE: Failure to close all the unused manifold
ports will decrease the vacuum level efficiency
of the rover.
0702-020-700 Rev-E
WARNINGS:
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