Stryker Neptune 3 User manual

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Instructions For Use
0703-001-700 C
0000160552, Rev. C Effective Date: Nov 25, 2015 1:43:15 PM
Print Date: Nov 25, 2015 02:19:13 PM
Item # 2

2015-11 0703-001-700 Rev-C www.stryker.com
Neptune®3 Waste Management System
120 VAC Rover
0703-001-000
Instructions For Use
ENGLISH (EN)
Software Version
002.003.xxx
0000160552, Rev. C Effective Date: Nov 25, 2015 1:43:15 PM
Print Date: Nov 25, 2015 02:19:13 PM

2 www.stryker.com
EN 0703-001-700 Rev-C
Failure to comply could result in
serious injury or death.
Only trained and experienced healthcare professionals may use
this equipment.
For more information, including safety information or in-service
training, contact your Stryker sales representative or call
Neptune Customer Service at 1-800-550-7836.
WARNING
DO NOT connect
directly to chest tubes.
DO NOT connect to
closed wound drains.
DO NOT connect directly
to tracheal tubes.
ALWAYS use the
minimum suction limit
required to achieve the
desired clinical outcome.
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0703-001-700 Rev-C EN
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Known Use Errors
It is important to acknowledge and be aware of potential hazards associated with high suction
devices prior to use. This information highlights known use errors that constitute improper and
unsafe use of a high suction device, such as the Neptune 3 Rover. Stryker has received incident
reports of serious injury and/or death associated with operating high suction devices.
Stryker has received reports that high suction devices have been connected directly to patients’
chest tubes, postoperatively, which resulted in deaths.
Stryker has received reports that high suction devices have been connected to patients’ closed
wound drains, postoperatively, which resulted in serious patient injuries.
Do not connect the Neptune 3 Rover directly to a patient’s chest tube.
Do not connect the Neptune 3 Rover to a closed wound drainage system.
For training information, visit www.neptunecustomercare.com.
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EN 0703-001-700 Rev-C
Contents
1 Introduction . . . . . . . . . . . . . . . . . . . . 7
1.1 Audience . . . . . . . . . . . . . . . . . . . 7
1.2 Conventions . . . . . . . . . . . . . . . . . . 7
1.3 Contact Information. . . . . . . . . . . . . . . 7
2 Indications For Use. . . . . . . . . . . . . . . . . 7
3 Contraindications . . . . . . . . . . . . . . . . . 7
4 Safety Directives . . . . . . . . . . . . . . . . . . 8
4.1 General Safety. . . . . . . . . . . . . . . . . 8
4.2 Connection Safety . . . . . . . . . . . . . . . 8
4.3 Suction Safety . . . . . . . . . . . . . . . . . 8
4.4 Electrical Safety . . . . . . . . . . . . . . . . 9
4.5 Environmental/Biological Safety . . . . . . . . . 9
5 System Overview. . . . . . . . . . . . . . . . . .10
5.1 Operation . . . . . . . . . . . . . . . . . . .10
5.2 Components and User Interface. . . . . . . . .12
5.3 For Use With. . . . . . . . . . . . . . . . . .13
5.4 Documentation. . . . . . . . . . . . . . . . .13
6 Features. . . . . . . . . . . . . . . . . . . . . .14
6.1 Hardware Interface . . . . . . . . . . . . . . .14
6.1.1 Rover Front View . . . . . . . . . . . . . .14
6.1.2 Rover Back View . . . . . . . . . . . . . .15
6.2 Software Interface . . . . . . . . . . . . . . .16
6.2.1 Safety Information Screens . . . . . . . . .16
6.2.2 Menu Structure. . . . . . . . . . . . . . .17
6.2.3 Screens, Dialogs, and Drop-downs. . . . . .18
6.2.3.1 Main Display Control Screen Areas . . .18
6.2.3.2 Typical Settings Dialog Areas . . . . . .19
6.2.3.3 Typical Docking Mode Screen Areas. . .20
6.2.3.4 Typical Notification or Error Drop-down
Areas . . . . . . . . . . . . . . . . . . . . .21
6.2.3.5 Top Display Screen Areas. . . . . . . .22
7 Definitions . . . . . . . . . . . . . . . . . . . . .23
8 Instructions . . . . . . . . . . . . . . . . . . . .28
8.1 Before First Use . . . . . . . . . . . . . . . .28
8.1.1 To Unpack the Rover . . . . . . . . . . . .28
8.1.2 To Add Canister Prefill Fluid. . . . . . . . .28
8.1.3 To Test the Rover. . . . . . . . . . . . . .28
8.1.3.1 To Connect Power to the Rover . . . . .28
8.1.3.2 To Test Fluid Suction . . . . . . . . . .28
8.1.3.3 To Test IV Pole Height Adjustment . . . .30
8.1.3.4 To Test Smoke Evacuation . . . . . . .30
8.1.4 To Adjust the Rover Settings . . . . . . . .31
8.2 Before the Procedure. . . . . . . . . . . . . .32
8.2.1 To Prepare the Rover. . . . . . . . . . . .32
8.2.2 To Install Disposable Components . . . . .33
8.2.2.1 To Prepare for Fluid Suction . . . . . .33
8.2.2.2 To Prepare for Smoke Evacuation . . . .34
8.2.2.3 To Prepare the IV Pole . . . . . . . . .34
8.3 During the Procedure . . . . . . . . . . . . .35
8.3.1 To Operate the Rover. . . . . . . . . . . .35
8.3.1.1 To Control Fluid Suction. . . . . . . . .36
8.3.1.2 To Control Smoke Evacuation . . . . . .36
8.3.1.3 To Manage a Full Canister . . . . . . .37
8.4 After the Procedure . . . . . . . . . . . . . .40
8.4.1 To Remove Disposable Components. . . . .40
8.4.1.1 To Remove Suction Components . . . .40
8.4.1.2 To Remove Evacuator Components . . .41
8.4.1.3 To Remove Fluid Bag(s) . . . . . . . .41
8.4.2 To Shut Down and Relocate the Rover . . .41
8.4.2.1 To Remove Power From the Rover. . . .41
8.4.2.2 To Prepare the Rover for Relocation . . .42
8.4.2.3 To Relocate the Rover . . . . . . . . .42
8.4.3 To Dock the Rover . . . . . . . . . . . . .42
8.4.3.1 To Prepare the Docker . . . . . . . . .43
8.4.3.2 To Perform a Docking Cycle . . . . . .43
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9 Inspection and Maintenance . . . . . . . . . . . .45
10 Cleaning and Disinfection . . . . . . . . . . . . .46
10.1 Recommended Equipment and Materials . . . .46
10.2 To Wipe Down the Rover . . . . . . . . . . .46
11 Storage and Handling . . . . . . . . . . . . . . .47
12 Disposal/Recycle . . . . . . . . . . . . . . . . .47
13 Troubleshooting . . . . . . . . . . . . . . . . . .48
13.1 Rover Operation. . . . . . . . . . . . . . . .48
13.2 Docking Station Operation . . . . . . . . . . .50
13.3 Troubleshooting Codes . . . . . . . . . . . .52
14 Specifications . . . . . . . . . . . . . . . . . .54
15 Electromagnetic Compatibility . . . . . . . . . . .56
16 Federal Communications Commission (FCC)
Statement Concerning Radio Frequency Interference . .58
16.1 Manifold Authentication . . . . . . . . . . . .58
16.1.1 FCC Compliance . . . . . . . . . . . . .58
16.1.2 Radio License . . . . . . . . . . . . . . .58
16.2 Docking Interface . . . . . . . . . . . . . . .58
16.2.1 FCC Compliance . . . . . . . . . . . . .58
17 Glossary . . . . . . . . . . . . . . . . . . . . .59
18 Software License Notices . . . . . . . . . . . . .59
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EN 0703-001-700 Rev-C
List of Tables
Table 1 – Components and Accessories . . . . . . . .13
Table 2 – Component Instructions for Use . . . . . . . 13
Table 3 – Control Screen Buttons . . . . . . . . . . .23
Table 4 – Symbols . . . . . . . . . . . . . . . . . .26
Table 5 – Suction Limit Ranges and Colors . . . . . .27
Table 6 – Title Area Colors . . . . . . . . . . . . . .27
Table 7 – Button Colors. . . . . . . . . . . . . . . .27
Table 8 – Manifold Symbol Colors . . . . . . . . . . .27
Table 9 – Canister Symbol Colors . . . . . . . . . . .27
Table 10 – Message Area Colors . . . . . . . . . . .27
Table 11 – Audible Event Indicators . . . . . . . . . .27
Table 12 – Abbreviations . . . . . . . . . . . . . . .27
Table 13 – Components Supplied with Rover . . . . . .28
Table 14 – Smoke Evacuator Modes of Operation . . .30
Table 15 – Rover Settings Options. . . . . . . . . . .31
Table 16 – High Suction Visual and Audible Indicators .36
Table 17 – Fluid Volume Indicators . . . . . . . . . .37
Table 18 – Docking Cycle Options. . . . . . . . . . .44
Table 19 – Inspection Schedule and Criteria . . . . . .45
Figure 39 – To Dispose of Suction Components . . . .41
Figure 40 – To Remove Evacuator Components . . . .41
Figure 41 – To Remove Fluid Bag(s). . . . . . . . . .41
Figure 42 – To Remove Power . . . . . . . . . . . .41
Figure 43 – Transport Configuration . . . . . . . . . .42
Figure 44 – To Prepare the Docker . . . . . . . . . .43
Figure 45 – To Dock the Rover . . . . . . . . . . . .43
Figure 46 – Docking Mode Screen - Normal Wash . . .44
Figure 47 – To Wipe Down the Rover . . . . . . . . .47
List of Figures
Figure 1 – To Collect Fluid Waste . . . . . . . . . . .10
Figure 2 – Fluid Stacking . . . . . . . . . . . . . .10
Figure 3 – To Empty the Canisters. . . . . . . . . . .10
Figure 4 – To Clean the Canisters . . . . . . . . . .11
Figure 5 – To Evacuate Surgical Smoke . . . . . . . .11
Figure 6 – To Adjust IV Pole Height . . . . . . . . . .11
Figure 7 – Components and Interface Diagram . . . . .12
Figure 8 – Rover Front View. . . . . . . . . . . . . .14
Figure 9 – Rover Back View. . . . . . . . . . . . . .15
Figure 10 – Top Display WARNING Screen . . . . . . .16
Figure 11 – Main Display WARNING Screen . . . . . .16
Figure 12 – Control Screen Menu Structure . . . . . . 17
Figure 13 – Roving Mode (Control) Screen . . . . . . .18
Figure 14 – Accessories Dialog . . . . . . . . . . . .19
Figure 15 – Docking Mode Screen. . . . . . . . . . .20
Figure 16 – Notification Drop-down . . . . . . . . . .21
Figure 17 – Top Display Screen . . . . . . . . . . . .22
Figure 18 – To Connect Power . . . . . . . . . . . .28
Figure 19 – Set Up System Screen . . . . . . . . . .29
Figure 20 – To Start and Adjust Fluid Suction . . . . .29
Figure 21 – To Test the Powered IV Pole . . . . . . . .30
Figure 22 – Evacuate Smoke Dialog . . . . . . . . . .30
Figure 23 – Settings Menu Dialog . . . . . . . . . . .31
Figure 24 – Preferences Dialog . . . . . . . . . . . .31
Figure 25 – To Connect Power . . . . . . . . . . . .32
Figure 26 – To Prepare for Fluid Suction . . . . . . . .33
Figure 27 – Reset Volumes Dialog. . . . . . . . . . .33
Figure 28 – To Prepare for Smoke Evacuation . . . . .34
Figure 29 – To Use the Powered IV Pole . . . . . . . .34
Figure 30 – To Start and Adjust Fluid Suction . . . . .36
Figure 31 – Almost Full Canister Condition . . . . . . .37
Figure 32 – Full Canister Condition . . . . . . . . . .38
Figure 33 – Empty 4-Liter Canister Dialog . . . . . . .38
Figure 34 – Emptying 4-Liter Canister Screen . . . . .38
Figure 35 – Prefilling 4-Liter Canister Screen. . . . . .38
Figure 36 – To Relocate the Manifold . . . . . . . . .39
Figure 37 – To Gather Suction Components . . . . . .40
Figure 38 – To Discontinue Fluid Suction . . . . . . .40
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1 Introduction
This instructions for use manual contains information
intended to ensure the safe, effective, and compliant use
of your product.
Keep and consult this reference manual during the life of
the product.
1.1 Audience
This manual is intended for in-service trainers, surgeons,
anesthetists, circulating nurses, surgical assistants,
biomedical equipment technicians, and housekeeping
staff.
1.2 Conventions
The following conventions are used in this manual:
WARNING A warning highlights a safety-related issue.
ALWAYS comply with this information to
prevent patient or healthcare staff injury.
CAUTION A caution highlights a product reliability
issue. ALWAYS comply with this
information to prevent product damage.
NOTE A note supplements and/or clarifies
procedural information.
1.3 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. Outside the US, contact your nearest
Stryker subsidiary.
2 Indications For Use
The Neptune 3 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.
3 Contraindications
The Neptune 3 Waste Management System is
contraindicated against:
▪ Connection directly to chest tubes.
▪ Connection to closed wound drainage systems.
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EN 0703-001-700 Rev-C
4 Safety Directives
4.1 General Safety
WARNINGS:
▪ Before using this equipment, or any component
compatible with this equipment, read and understand
the instructions for use. Pay particular attention to
safety information. Become familiar with the equipment
before use.
▪ Only healthcare professionals trained and experienced
in the use of this medical device should operate this
equipment.
▪ Healthcare professionals should be thoroughly
familiar with the instructions for use, performance
characteristics, and the indicated, contraindicated, and
intended uses of this equipment. Contact your Stryker
sales representative or Stryker Neptune Customer
Service for in-service training. See Section 1.3 Contact
Information.
▪ The healthcare professional performing any procedure
is responsible for determining the appropriateness of
this equipment and the specific technique used for
each patient. Stryker, as a manufacturer, does not
recommend surgical procedure or technique.
▪ DO NOT disassemble, modify, service, or repair
any equipment without the authorization of the
manufacturer. Call Stryker Neptune Customer Service.
See Section 1.3 Contact Information.
▪ Upon initial receipt and before each use, inspect each
component for damage. DO NOT use any equipment if
damage is apparent or the inspection criteria are not
met. See Table 19 Inspection Schedule and Criteria.
▪ ALWAYS operate the equipment within the specified
environmental condition values. See Section 14
Specifications.
▪ The collection canister scale, top display, and main
display are not diagnostic tools. DO NOT use the scale
or either display to determine the amount of fluid lost
from or retained by the patient.
▪ DO NOT cover the top display or main display with
drapes or other objects. ALWAYS make sure the top
display and main display can be clearly seen.
4.2 Connection Safety
WARNINGS:
INAPPROPRIATE CONNECTION HAZARD
▪ DO NOT connect directly to chest tubes.
▪ DO NOT connect to closed wound drains.
▪ DO NOT connect directly to tracheal tubes.
▪ NOT FOR USE as a suction source for:
– Intermittent suction applications
– Patient positioner devices
– Organ stabilizer/positioner devices
Death or serious injury can result from inappropriate
connections.
4.3 Suction Safety
WARNINGS:
HIGH SUCTION HAZARD [MAX = 520 mm-Hg]
▪ The effectiveness of aspiration is dependent upon the
intensity of the suction applied.
▪ ALWAYS use the minimum suction limit range required
to achieve the desired clinical outcome.
▪ ALWAYS follow your institution’s guidelines for suction
limits.
▪ The suction limit range of each collection canister
may be adjusted by the appropriate suction control
dial on the control panel. Interruption and restoration
of rover power while suction is ON, whether accidental
or intentional, does not reset the suction limit range to
zero. See BS EN ISO 10079-1: 2009, clause 13.8. Use
caution when activating suction with a high suction
limit range.
Death or serious injury can result from improper suction
levels.
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4.4 Electrical Safety
WARNINGS:
ELECTROMAGNETIC INTERFERENCE HAZARD
▪ Use only Stryker-approved electronic components
and accessories. Failure to comply may result in
increased electromagnetic emissions or decreased
electromagnetic immunity of the system.
▪ Take special precautions regarding electromagnetic
compatibility (EMC) when using this medical electrical
equipment. Install and place this medical electrical
equipment into service according to the EMC
information contained in this manual. See Section 15
Electromagnetic Compatibility. Portable and mobile
radio frequency (RF) communications equipment
can affect the function of this medical electrical
equipment.
ELECTRICAL SHOCK HAZARD
▪ ALWAYS connect this equipment to a hospital-
grade, facility power receptacle with protective earth
(ground).
▪ DO NOT touch or make contact with the rover and
patient simultaneously.
Failure to comply may cause electrical shock and result in
patient or healthcare staff injury.
4.5 Environmental/Biological Safety
WARNINGS:
FIRE HAZARD: DO NOT use this equipment in areas in
which flammable anesthetics or flammable agents are
mixed with air, oxygen or nitrous oxide. Failure to comply
may cause a fire and result in burn injury or property
damage. See BS EN ISO 10079-1: 2009, clause 9.4.
BLOODBORNE PATHOGEN HAZARD
▪ The Bloodborne Pathogens Standard provided by
the United States Occupational Safety and Health
Administration (US OSHA 29 CFR 1910.1030) requires
those employers with employees having occupational
exposure to potentially infectious materials to establish
a written Exposure Control Plan. The Exposure Control
Plan is designed to eliminate or minimize employee
exposure through use of personal protective equipment
(PPE), appropriate vaccinations (for example, hepatitis
B), and other control measures.
▪ ALWAYS wear PPE when operating or handling this
equipment.
▪ ALWAYS follow local regulations regarding proper
handling and disposal of biohazard waste.
Failure to comply may cause infection and result in
healthcare staff injury.
CONTAMINATION HAZARD
▪ DO NOT collect fluids from patients being treated with
radioisotopes or hazardous chemical agents.
▪ ALWAYS follow local regulations for safe handling,
recycling, and disposal of biohazard fluid waste and
equipment. See Section 12 Disposal/Recycle.
Failure to comply may cause environmental contamination
and result in injury.
INFECTION HAZARD
▪ ALWAYS clean and disinfect the equipment as
indicated upon initial receipt and before each use.
▪ DO NOT place the rover within the sterile field.
▪ DO NOT reuse, reprocess, or repackage a manifold
that is intended for single use only.
– A single use device may not withstand chemical,
chemical vapor, or high temperature sterilization
reprocessing.
– Design features may make cleaning and
disinfection difficult.
– Reuse may create a contamination risk or
compromise structural integrity resulting in
operational failure.
– Critical product information may be lost during
repackaging.
Failure to comply may lead to infection or cross infection
and result in patient and/or healthcare staff injury.
FLUID WASTE LEAKAGE HAZARD: ALWAYS make sure
rover power is ON when collecting fluid waste. The rover
can only detect full canisters if the rover power is ON. If
rover power is OFF, fluid waste leakage can occur.
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5 System Overview
5.1 Operation
The Stryker Neptune 3 Rover (rover) is a mobile unit used
to suction and collect fluid waste and evacuate surgical
smoke from a surgical site. The rover also has a height-
adjustable, powered IV pole.
During collection, fluid waste is removed from the surgical
site through suction tubing connected to inlet ports
of manifold(s) installed in the rover. The fluid waste is
collected in the canister(s) of the rover (Figure 1). The
two-canister design allows separate suction limit ranges
and fluid volume measurement capability. However, both
canisters use a single vacuum pump. The vacuum pump
exhaust and canister exhaust are filtered.
Figure 1 – To Collect Fluid Waste
Manifolds and suction tubing are single-use disposables
and must be replaced between patients. However, it may
not be necessary to empty the contents of the rover’s
collection canisters.
If the rover display indicates sufficient fluid volume
capacity in one or both canisters, the rover may be used
for additional surgical procedures. This concept is known
as fluid stacking (Figure 2). See Section 17 Glossary.
Figure 2 – Fluid Stacking
After collection, the rover is relocated and connected to
the Stryker Docking Station (docker). Once the rover is
connected to the docker, the emptying of the fluid waste
and cleaning of the canisters occurs automatically
(Figure 3).
Figure 3 – To Empty the Canisters
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The rover canisters are rinsed with clean water and
Neptune Docking Detergent REF 0700-001-026 to clean
the canisters of any residual fluid waste (Figure 4).
Figure 4 – To Clean the Canisters
Surgical smoke may also be evacuated from the surgical
site through smoke tubing connected to the smoke
evacuator filter installed in the rover. The surgical smoke
is filtered inside the rover (Figure 5).
Figure 5 – To Evacuate Surgical Smoke
The height of the IV pole may be adjusted by touching
and holding buttons on the control screen (Figure 6).
Figure 6 – To Adjust IV Pole Height
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5.2 Components and User Interface
A complete Neptune Waste Management System consists of a rover with an installed fluid suction High Efficiency Particulate
Air (HEPA) filter, a docker, and various single-use, disposable devices, including one manifold per collection canister, and
fluid suction tubing. A smoke evacuator Ultra Low Penetration Air (ULPA) filter and smoke evacuator tubing may also be
required (Figure 7). See Section 5.3 For Use With.
The user interface provides complete control over functionality and provides audible, visual, and tactile feedback of status.
The user interface elements include one main display with touch capability, two suction control dials, two manifold receptacle
suction indicators and one top display (Figure 7, Figure 8, and Figure 9).
Speaker
Suction
Dials
ROVER
DOCKER
Communication
Window
Docker
Interface
Communication
Windows
Required Components User Interface
Rover
Interface
Manifold Fluid
Tubing
Smoke
ULPA Filter
Smoke
Tubing
Manifold Fluid
Tubing
Top
Display
QRC
Suction
HEPA Filter
4 L
Canister
20 L
Canister
Touch
Display
Suction Indicator
Suction Indicator
Figure 7 – Components and Interface Diagram
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5.3 For Use With
Table 1 – Components and Accessories
This table identifies required components and optional
accessories used with the rover to accomplish its
intended use. Components and accessories are sold
separately.
DESCRIPTION REF
Docking Station
Neptune 2 Docking Station (120 VAC) 0702-014-000
Docking Station Accessory
Neptune Docking Detergent (2/pack) 0700-001-026
Fluid Filter
Fluid Suction HEPA Filter (1 each) 0702-034-000
Manifold(s)
Four-port Manifold (20/pack) 0702-020-000
Single-port Manifold (20/pack) 0702-025-000
Four-port Manifold with Specimen
Collection (20/pack)
0702-020-001
Fluid Suction Tubing
Medical grade fluid suction tubing with
3/8 inch connector
Commercially
available
Smoke Filter
Smoke Evacuator ULPA Filter (4/pack) 0702-040-000
Smoke Tubing
Medical grade smoke evacuator tubing
with a 1/4 inch, 3/8 inch, or 7/8 inch
connector
Commercially
available
Smoke (Evacuator)Tubing, 3/8 inch x
10 feet (10/pack)
0702-045-023
Smoke (Evacuator) Tubing, 7/8 inch x
10 feet (10/pack)
0700-025-000
Smoke (Evacuator) Tubing, 7/8 inch x
10 feet with Wand (10/pack)
0700-026-000
NOTE: For a complete list of components and
accessories or ordering information, contact your Stryker
sales representative or call Stryker Neptune Customer
Service. See Section 1.3 Contact Information. Outside the
US, contact your nearest Stryker subsidiary.
5.4 Documentation
Table 2 – Component Instructions for Use
This table identifies the instructions for use supplied with
required components.
Instructions for Use REF
Neptune 2 Docking Station 0702-014-700
Disposable Manifolds 0702-020-700
Fluid Suction HEPA Filter 0702-034-700
Smoke Evacuator ULPA Filter 0702-040-700
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EN 0703-001-700 Rev-C
6 Features
6.1 Hardware Interface
6.1.1 Rover Front View
C
B
A
J
D
E
F
G
H
K
I
Figure 8 – Rover Front View
A Docking Station Interface (not shown) –
Provides a sealed flow path for fluid waste
transfer from the rover to the docker. Also
provides fresh water and detergent transfer from
the docker to the rover canisters.
B Infrared Communication Window – Allows data
transfer between the docker and rover during the
docking procedure. See Section 17 Glossary for
the definition of infrared communication.
C 20L (20-liter) Canister – Allows for the collection
and containment of fluid waste. The 20-liter
canister receives fluid through an installed
manifold during collection. The canister contains
a fluid level sensor to provide volume information
to the top and main displays. See Section 8.3.1.3
To Manage a Full Canister. See Section 17
Glossary for the definition of a fluid level sensor.
D 4L (4-liter) Canister – Allows for the collection
and containment of fluid waste. The 4-liter
canister receives fluid through an installed
manifold during collection. The canister contains
a fluid level sensor to provide volume information
to the top and main displays. The contents of the
4-liter canister may be emptied into the 20-liter
canister.
E High Suction Device WARNING Label (two) -
WARNING
HIGH SUCTION DEVICE
DO NOT connect directly to
chest tubes or other closed
wound drains.
Failure to comply could result
in serious injury or death.
F Manifold Receptacle (two) – Allows installation
of a disposable manifold into the canister. The
installation or removal of a valid manifold enables
or disables suction, respectively. See Section
17 Glossary for the definitions of a valid and
invalid manifold. The receptacle port will close
automatically when a manifold is removed.
Closure prevents fluid waste leakage from the
canister and prevents foreign objects from
entering the canister.
G Suction Range Indicator (two) – Provides color-
coded visual information about the suction limit
range. See Table 5 Suction Limit Ranges and
Colors.
H Speaker – Located inside the rover; provides
audible event indicators. See Table 11 Audible
Event Indicators.
I Quick Reference Card (QRC) – Allows for
quick access to warnings and troubleshooting
information.
J Height Adjustable, Powered IV Pole with Four
Hooks – This IV pole is capable of supporting
one three-liter [3000 mL] fluid bag per hook.
The powered IV pole will return to its lowest
position automatically when power is removed
from the rover, to ensure proper clearance during
relocation.
K Top Display – Provides visual information of
status, as well as safety and alarm indications
(Figure 10 and Figure 17). The display swivels
in a 360-degree fashion and pivots for ease of
viewing from the surgical field or control panel.
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6.1.2 Rover Back View
L
Q
M
N
V
W
U
T
S
O
Z
AA
AB
Y
X
R
P
Figure 9 – Rover Back View
L Vacuum Pump (not shown) – Creates suction
for both canisters. If the suction level decreases
in either canister due to an open manifold port,
the suction level in the other canister may
decrease.
M Fluid Suction Filter Compartment – Allows
for the installation and removal of a disposable
fluid suction filter. This filter (included) provides
HEPA filtration of the air from the 20-liter and
4-liter canisters. See Section 9 Inspection and
Maintenance.
N Canister Viewing Door/Handle (four) – Each
canister has two viewing doors with a handle.
These doors may be opened during operation to
reveal the contents or closed during relocation to
conceal the contents.
O Smoke Evacuator Filter Compartment – Allows
for the installation and removal of a disposable
smoke evacuator filter (not included) with an
ULPA efficiency rating.
P HIGH VACUUM/HIGH FLOW Continuous
Surgical Suction Range: 50 to 520 mm-Hg, –
See Section 14 Specifications.
Q Control Panel – Consists of a touch-sensitive
main display and two suction control dials.
R Main Display – Provides the primary operating
interface via a touch-sensitive control screen.
The display also provides important status
information and alarm status (Figure 11 and
Figure 13).
S 4-Liter Suction Control Dial – Allows for the
rotary adjustment of the suction LIMIT value of
the 4-liter canister; clockwise increases the value
and counterclockwise decreases the value. The
suction value will appear on the main display as
a LIMIT value. See Table 5 Suction Limit Ranges
and Colors.
T 20-Liter Suction Control Dial – Allows for the
rotary adjustment of the suction LIMIT value of
the 20-liter canister; clockwise increases the
value and counterclockwise decreases the value.
The suction value will appear on the main display
as a LIMIT value. See Table 5 Suction Limit
Ranges and Colors.
U Handle – Allows for relocation and positioning of
the rover.
V Manifold Holder – Allows for the storage of new,
unused manifolds.
W Power Cord Receptacle/Switch – Allows for the
connection and application of facility power to
the rover.
X Serial Number Label – Identifies the serial
number information of the rover.
Y Specification Label – Identifies the part
number information of the rover. See Section 14
Specifications.
Z Power Cord Bracket – Allows for the wrapping
and storage of the supplied power cord.
AA Power Cord with Retainer – The supplied power
cord is used to connect the rover to facility
power. The retainer keeps the cord in place.
AB Casters (four) – Four swivel casters provide
mobility for the rover to roll across a floor.
The two rear casters have locks to prevent
unintended movement during operation.
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16 www.stryker.com
EN 0703-001-700 Rev-C
6.2 Software Interface
6.2.1 Safety Information Screens
Failure to comply could result in serious injury or death
DO NOT connect directly
to chest tubes.
DO NOT connect to closed
wound drains.
WARNING
Figure 10 – Top Display WARNING Screen
Failure to comply could result in serious injury or death.
DO NOT connect
directly to chest
tubes.
DO NOT connect
to closed wound
drains.
DO NOT connect
directly to
tracheal tubes.
ALWAYS use the
minimum suction
limit required to
achieve the
desired clinical
outcome.
ConfirmI have read and understand the safety warnings
WARNING 002.003.000
Figure 11 – Main Display WARNING Screen
NOTE: The software version number appears in the upper right corner of the main display WARNING screen. Make sure the
number on the screen matches the software version number on the cover of this instructions for use. If not, contact your
Stryker sales representative or call Stryker Neptune Customer Service to obtain the latest instructions for use manual. See
Section 1.3 Contact Information.
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0703-001-700 Rev-C EN
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6.2.2 Menu Structure
The main display control screen has a menu structure that provides access to the primary control functions (Figure 12).
Evacuate
Smoke
IV Pole
Power
Reset
Volumes
Settings
Start Suction
4L Light
Empty 4L
Canister
Stop Suction
Normal Wash
Quick Wash
Extended
Wash
Manifolds
Filters
Display
Sounds
Lights
Docking
Preferences
Accessories
On
Auto
Off
Figure 12 – Control Screen Menu Structure
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18 www.stryker.com
EN 0703-001-700 Rev-C
6.2.3 Screens, Dialogs, and Drop-downs
6.2.3.1 Main Display Control Screen Areas
Suction ON
Evacuate Smoke
Reset Volumes
Settings
4L Light
Empty 4L
Canister
4 L Suction Limit
50
mm-Hg
44
Actual:
mm-Hg
used
used
Stop Suction
OFF
MAX
HIGH
MED
LOW
200 mL
since last reset
0 mL
since last reset
120
mm-Hg
115
Actual:
mm-Hg OFF
MAX
MED
LOW
HIGH
20 L HIGH suction
C D FE HG
I
J
K
B
A
Figure 13 – Roving Mode (Control) Screen
A Suction Control Area – Provides a toggle
button to control the presence or absence of
fluid suction.
B Control Menu Area – Provides buttons to
control the primary functions of the rover
(Figure 12).
C Notification Message Area – Indicates when
a low priority alarm condition has occurred
(Figure 16); touch to access the drop-down list
and/or message. See Section 17 Glossary.
D Error Message Area – Indicates when a
medium priority alarm condition has occurred;
touch to access the drop-down list and/or
message. See Section 17 Glossary.
E Canister Information Area (two) – Identifies
the specific canister; also provides fluid volume
information via a 4L or 20L canister symbol
and a fluid volume reading. If the canisters’
volumes are reset, the words ‘since last reset’
will appear. See Table 9 Canister Symbol
Colors.
F Suction Status Area (two) – Indicates
the suction status of a canister, including
STOPPED, PAUSED, or HIGH.
G Manifold Indicator Area (two) – Indicates
the status of the manifold installed in the
receptacle. Status conditions include new or
used. See Table 8 Manifold Symbol Colors.
H Title Area – Indicates status, including system
setup, suction ON, suction OFF, EMPTYING
4-liter canister, and PREFILLING 4-liter
canister. See Section 17 Glossary for the
definition of prefilling.
I Suction Gauge Area (two) – Indicates the
suction selected with the rotary suction control
dial, including OFF, LOW, MEDium, HIGH, or
MAXimum. See Table 5 Suction Limit Ranges
and Colors.
J Suction LIMIT Value Area (two) – Indicates
the selected suction limit value obtained by
using the rotary suction control dial.
KACTUAL Suction Value Area (two) – Indicates
the actual suction value present in the canister.
The ACTUAL value may fluctuate and could be
significantly lower than the suction LIMIT value.
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6.2.3.2 Typical Settings Dialog Areas
Back Close
Accessories
Filters
Fluid Suction HEPA Filter
Time remaining (out of 500)
497 hours
Smoke Evacuation ULPA Filter
Time remaining (out of 80)
80 hours
Manifolds
Reset
hours
Reset
hours
D
E
C
B
A
Figure 14 – Accessories Dialog
A Navigation Area – Provides buttons used to
return to the SETTINGS dialog menu or control
screen.
B Options Area – Provides options that may be
adjusted, as well as default settings information
or life-cycle use information.
C Tab Selection Area – Provides selection tabs,
including FILTERS, MANIFOLDS, SOUNDS,
DISPLAYS, and LIGHTS.
D Title Area – Indicates the name of the settings
dialog, including DOCKING, ACCESSORIES,
and PREFERENCES.
E Option Adjustment Area(s) – Provides buttons
used to adjust sound or brightness, reset
hours, or select default settings. Also displays
the number of manifolds used within the last
30 days and 90 days.
0000160552, Rev. C Effective Date: Nov 25, 2015 1:43:15 PM
Print Date: Nov 25, 2015 02:19:13 PM