Stryker 7110-190-000 User manual

2020-08 7110-120-700 Rev-AB www.stryker.com
Instructions For Use
ENGLISH (EN)
Universal Battery Charger
REF
REF
7110-120-000
Stryker F1®Universal
Battery Charger
REF
REF
7110-190-000

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EN 7110-120-700 Rev-AB
Safety Directives
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.
• The Stryker Universal Battery Charger
and Stryker F1 Universal Battery Charger
are limited to professional use within a
professional healthcare environment, excluding
near high frequency (HF) surgical equipment
and accessories. See the Electromagnetic
Compatibility section.
• Upon initial receipt and before each use,
operate the equipment and inspect each
component for damage. DO NOT use any
equipment if damage is apparent. See the
Inspection and Testing section for inspection
criteria.
• DO NOT use this equipment in areas in which
flammable anesthetics or flammable agents
are mixed with air, oxygen, or nitrous oxide.
• Take special precautions regarding
electromagnetic compatibility (EMC) when
using medical electrical equipment. Place this
equipment into service according to the EMC
information contained in this manual. Portable
and mobile radio frequency (RF) equipment
can affect the function of this equipment.
• ALWAYS use the appropriate battery charger to
charge battery packs.
• DO NOT operate the battery charger using a
voltage inconsistent with the rating on the back
of the unit.
• DO NOT operate the battery charger with a
damaged power cord or plug.
Introduction
This instructions for use manual contains
information intended to ensure the safe, effective,
and compliant use of your product. This manual is
intended for 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.
For additional information, including safety
information, in-service training, or current literature,
contact your Stryker sales representative or call
Stryker customer service at 1-269-323-7700 or
1-800-253-3210. 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.
Trademarks not the property of Stryker
Corporation are the property of their respective
owners.
Indications For Use
The Stryker Universal Battery Charger and Stryker
F1 Universal Battery Charger (battery chargers)
are four-station, modular battery chargers intended
to charge Stryker handpiece battery packs only.
The battery chargers and battery packs are
specifically designed to work together so that the
battery charger’s information screen will provide
specific battery pack information.
Contraindications
None known.

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The following Stryker-approved accessories are sold separately:
CHARGER MODULE REF FOR USE WITH BATTERY PACK REF
Charger Module* 6110-412-000 4112-000-000
System 5 Module 6110-415-000 4115-000-000
Charger Module 6110-422-000 4212-000-000
4215-000-000
Non-sterile Battery Charger
Module
6110-426-000 4126-110-000
4222-110-000
System 6 Module 6110-625-000 6126-110-000
6212-000-000
6215-000-000
7126-110-000
7212-000-000
7215-000-000
7222-110-000
8212-000-000
8215-000-000
Stryker F1 Charger Module 1900-125-000 1900-012-000
1900-013-000
*This charger module is not design integrated. The battery charger will not display charge cycle count
information for this charger module.
POWER CORD REF
Source Cord 0277-702-019
European Source Cord 0590-100-002
Power Cord (general) 0996-851-XXX series
Accessories
WARNINGS:
• Use only Stryker-approved equipment, unless
otherwise specified.
• DO NOT modify any equipment without the
authorization of the manufacturer.
• Use only Stryker-approved electronic
components and accessories. Failure to
comply may result in degraded performance,
increased electromagnetic emissions, or
decreased electromagnetic immunity of the
system.
• DO NOT use any battery charger accessory
that is not recommended or sold by Stryker.
Failure to comply may result in fire, electric
shock, or injury.
CAUTION: ALWAYS select and install the
appropriate charger module for the specific
battery pack used.
NOTES:
• Four System 6™ Modules (REF 6110-625-
000) are supplied with the Universal Battery
Charger.
• Four Stryker F1 Charger Modules (REF 1900-
125-000) are supplied with the Stryker F1
Universal Battery Charger.
• Alternative charger modules may be installed
to accommodate specific types of battery
packs as required.
• For a complete list of accessories, contact
your Stryker sales representative. Outside the
US, contact your nearest Stryker subsidiary.

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EN 7110-120-700 Rev-AB
Features
Battery Charger
C
D
E
FG
HI
J
A
B
A Battery Pack – A variety of battery
packs are sold separately.
B Charger Module – An interchangeable
component designed to accept a
specific type of battery pack. A
variety of charger modules are sold
separately.
C Indicator Lights – Provide status
information for each charger module.
D Information Screen – Provides status
information and error messages for the
battery charger, charger modules, and
battery packs.
E Input Buttons – Allow the user to
interact with the battery charger. The
information screen displays appropriate
input button labels during the battery
pack charging sequence.
F Power Cord Receptacle – Accepts the
power cord.
G Power Cord – Connects the battery
charger to a hospital-grade, facility
power receptacle
H Isolated Diagnostics Port – An
Ethernet receptacle used to export
device usage data from the battery
charger to Stryker via Stryker’s Cloud,
if desired.
I Ethernet Cable (not supplied) –
Connects the isolated diagnostics port
to a facility Ethernet receptacle
J MAC ID Label – Shows the Media
Access Control Identifier (MAC
Address) for the battery charger.

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Information Screen
AB
DE
C
A State-of-Health Area – Indicates
charging activity, and the state-of-
health of the battery pack.
B Counter Area – Displays numeric
information based on the state of the
battery charger, charger modules, and/
or battery packs.
C Message Area – Displays status
information and requests user action.
D Symbol Area – Displays symbols
based on the state of the battery
charger, charger modules, and/or
battery packs.
E Input Button Label Area – Displays
appropriate input button labels during
the battery pack charging sequence.
Indicator Lights
INDICATION STATUS
GREEN
(Steady State)
The battery pack is fully
charged.
AMBER
(Steady State)
The battery charger is either
charging or discharging the
battery pack.
AMBER
(Slow Blinking)
The battery pack is at or
near the end of its useful life.
AMBER
(Fast Blinking)
The battery charger or
charger module failed
diagnostic testing.
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
REPLACE – The battery pack
failed the state-of-health test.
Ethernet
MAC ID Media Access Control Identifier
Stryker F1 battery pack orientation
Refer to instruction manual/booklet
General warning sign
CSA Group certification mark
for United States and Canada.
These products were tested and
meet medical electrical equipment
certification requirements,
including compliance with
applicable 60601 series standards.
For additional information, contact
Stryker.

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EN 7110-120-700 Rev-AB
Instructions
To Connect the Battery Charger
WARNINGS:
• To avoid the risk of electric shock, ALWAYS
connect this equipment to a hospital-grade,
facility power receptacle with protective earth.
• DO NOT modify the power cord.
• ALWAYS position the equipment so that the
power cord may be easily disconnected as
required.
• DO NOT place the battery charger within the
sterile field.
• DO NOT touch the battery charger and the
patient simultaneously. Failure to comply may
cause electrical shock.
CAUTION: ALWAYS place the power cord where it
will not be stepped on, tripped over, or otherwise
subjected to damage or stress.
1. Use the power cord to connect the battery
charger to a hospital-grade, facility power
receptacle (figure 1). The power-up sequence
will begin:
- A diagnostic test will be performed to
ensure the battery charger and each
installed charger module is operational
- The battery charger software and hardware
revision numbers will appear (figures 2
and 3)
- The charger module revision number will
appear for each installed charger module
(figure 4).
NOTE: If an ERROR message appears during
the power-up sequence, note the error code that
appears in the counter area (figure 5). See the
Troubleshooting section.
2. If desired, use an Ethernet cable (not
supplied) to connect the isolated diagnostics
port to a facility Ethernet receptacle.
NOTES:
• Confirm with a facility IT representative
that the Ethernet receptacle has access to
Stryker’s Cloud.
• See the Network Requirements in the
Specifications section.
• For more information, contact your Stryker
sales representative.
Figure 1 – Battery Charger Connections
Figure 2 – Software Revision Number
Figure 3 – Hardware Revision Number
Figure 4 – Charger Module Revision Number
Figure 5 – Error Code

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To Charge a Battery Pack
CAUTION: When battery packs require
postsurgical sterilization, ALWAYS allow the battery
packs to cool for one hour before charging.
Excess heat buildup from sterilization and
charging will damage the battery packs.
NOTES:
• To ensure maximum operating time, always
charge battery packs before sterilization, even
if the battery packs have not been used.
• The charging sequence may take between
5 and 120 minutes, based on the type of
battery pack and the existing level of charge in
the battery pack.
• On the Stryker F1 Universal Battery Charger,
always install Stryker F1 SmartGrip®Battery
Modules in the proper orientation (figure 6).
Figure 6 – Stryker F1 SmartGrip Battery
Module Orientation
1. Install a clean, dry battery pack into a
compatible charger module with a NO
BATTERY message screen (figure 7).
The information screen will momentarily
display the battery pack part number (figure 8)
and the charging sequence will begin.
During the charging sequence, a CHARGING
message will appear and the number of
illuminated state-of-health bars will increase
from left to right (figure 9).
After the battery pack is fully charged, a state-
of-health test will be performed (figure 10):
- Five to eight bars will illuminate in the
state-of-health area. More illuminated bars
indicates a better ability of the battery
pack to store energy.
- The counter area will update the charge
cycle count (for design integrated
components only).
- A READY message will appear.
Figure 7 – No Battery Message
Figure 8 – Battery Pack Part Number
Figure 9 – Charging Message and Bars
Figure 10 – Ready Message with State-of-
Health Bars and Charge Cycle Count

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EN 7110-120-700 Rev-AB
Figure 11 – Replace Message and Symbol
Figure 12 – Total Number of
Over Temperature Events
Figure 13 – Total Time Exposed to
Over Temperature Conditions
Cleaning
To Clean the Battery Charger and
Charger Modules
WARNING: Before cleaning, ALWAYS
disconnect the power cord from the facility
power receptacle and the battery charger
to reduce the risk of electric shock.
CAUTIONS:
• DO NOT immerse the battery charger or
charger modules in liquid.
• DO NOT use solvents, lubricants, or other
chemicals to clean the battery charger or
charger modules unless otherwise directed.
NOTE: If the battery pack fails the state-of-health
test, a REPLACE message and symbol will appear
(figure 11). See the Troubleshooting section.
2. Store the battery pack on the battery charger
to maintain a full charge before sterilization.
To Access Over Temperature
Information
NOTES:
• Specific types of battery packs allow you
to access information about battery pack
exposure to over temperature conditions.
• The information screen will return to its origin
after displaying an over temperature message
screen for five seconds.
1. From the READY, CHARGING, or REPLACE
message screen, press the MORE button to
access the # of OVER TEMP message screen.
The counter will display the number of times
the battery pack has been exposed to an over
temperature condition (figure 12).
2. Press the MORE button again to access the
TIME OVER TEMP message screen. The
counter will display how much time, in minutes,
the battery pack has been exposed to over
temperature conditions (figure 13).
To Disconnect the Battery Charger
CAUTION: To reduce the risk of damage to the
power cord, ALWAYS pull the power cord plug, not
the power cord when disconnecting the battery
charger.
Disconnect the battery charger from the facility
power receptacle and Ethernet receptacle, as
required.
To Replace a Charger Module
See the instructions for use supplied with the
replacement charger module.

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• The use of abrasive disinfectants, such as
Clorox bleach, can lead to build-up on the
contacts which may affect the functionality of
the charger module.
• DO NOT allow liquid to collect in the charger
modules or on top of the battery charger.
• DO NOT allow liquid to enter the cooling vents
on the back of the battery charger.
• DO NOT spray or wipe liquid directly on the
contacts of the charger modules.
• DO NOT sterilize the battery charger or
charger modules.
1. Disconnect the power cord from the facility
power receptacle and the battery charger.
2. Disconnect the Ethernet cable, if used, from
the isolated diagnostics port.
3. Gently wipe the external surfaces of the
battery charger and power cord with a soft,
lint-free cloth moistened with a prepared
cleaning solution or non-abrasive, hospital
disinfectant and water.
4. Immediately dry the battery charger with
a soft, lint-free cloth or compressed air,
< 140 kPa [< 20 psi].
5. Inspect the battery charger and power cord
for damage. See the Inspection and Testing
section for inspection criteria.
To Clean the Battery Pack
For battery pack processing instructions, see the
care instructions manual supplied with the battery
pack and/or a compatible handpiece.
Inspection and Testing
WARNINGS:
• Only individuals trained and experienced in
the maintenance of reusable medical devices
should inspect and test this equipment.
• Before attempting any inspection and testing,
ALWAYS disconnect the power cord from the
battery charger to reduce the risk of electric
shock.
• Perform recommended inspection and testing
as indicated in these instructions.
• DO NOT use any equipment if damage is
apparent.
• DO NOT use any system component if the
inspection criteria are not met.
• DO NOT disassemble or service this
equipment. Failure to comply may result in
electric shock or fire.
NOTES:
• If the equipment fails to meet the inspection
and testing criteria, contact your Stryker sales
representative or call Stryker customer service.
Outside the US, contact your nearest Stryker
subsidiary.
• Maintenance documentation for this equipment
is available upon request to Stryker-authorized
service personnel only.
INTERVAL ACTIVITY CRITERIA
Upon initial
receipt and
before each
use
Inspect the
equipment
No damage or
signs of wear
No loose
or missing
components
No cuts in the
power cord
No bent pins or
contacts
No cracks in the
housing
Storage and Handling
CAUTION: ALWAYS store the equipment within
the specified environmental condition values
throughout its useful life. See the Specifications
section.
To ensure longevity, performance, and safety,
use of the original packaging materials is
recommended when storing or transporting this
equipment.

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EN 7110-120-700 Rev-AB
Disposal/Recycle
WARNING: 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.
In accordance with European Directive 2012/19/EU on Waste Electrical and Electronic
Equipment (WEEE) as amended, product should be collected separately for recycling.
Do not dispose of as unsorted municipal waste. Contact local distributor for disposal
information. Ensure infected equipment is decontaminated prior to recycling.
NOTE: Contact Stryker for the recycling passport for this product.
China RoHS Standard SJ/T 11364
To comply with China RoHS Standard SJ/T 11364, this device has been marked with
the environmentally-friendly use period (EFUP) number, measured in years. The device
contains at least one of the listed hazardous substances above threshold.
China RoHS Disclosure Report
REF 7110-120-000, REF 7110-190-000
Part Name
Hazardous Substances
Lead
(Pb)
Mercury
(Hg)
Cadmium
(Cd)
Hexavalent
Chromium
(Cr (VI))
Polybrominated
biphenyls
(PBB)
Polybrominated
diphenyl ethers
(PBDE)
Electronic
Circuit Boards X O O O O O
This table is prepared in accordance with the provisions of SJ/T11364.
O: Indicates that said hazardous substance contained in all of the homogenous materials for this part
is below the limit requirement of GB/T26572.
X: Indicates that said hazardous substance contained in at least one of the homogenous materials
used for this part is above the limit requirement of GB/T26572.