ICU Medical 20791 User Manual
Hospira MedNet 802.11 a/b/g Wireless
Upgrade Module
Connectivity Engine (CE)
Configuration Guide
Includes
®
*Hospira MedNet
For Use with Plum A+ Infusers (Lists 11971, 12391, 20679 & 20792-04)
*Hospira MedNet
Plug ‘n Play Module (List 20677 & 20791-04-77)
®
Software (List 16033-04)
430-11541-001
©
Hospira, Inc.
This document and the subject matter disclosed herein are proprietary information.
Hospira retains all the exclusive rights of dissemination, reproduction, manufacture, and sale.
Any party using this document accepts it in confidence, and agrees not to duplicate it in whole
or in part nor disclose it to others without the written consent of Hospira.
430-11541-001 CE Configuration Guide
Change History
Part Number Description of Change
430-11541-001
(Rev. 01/07)
Original issue
CE Configuration Guide i 430-11541-001
CHANGE HISTORY
This page intentionally left blank.
430-11541-001 ii CE Configuration Guide
Contents
INTRODUCTION TO THE MEDNET WIRELESS MODULE - - - - - - - - - - - - - - - - - - - - 1
FCC INFORMATION - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1
US FCC (F
FCC I
R
ADIO FREQUENCY EXPOSURE STATEMENT - - - - - - - - - - - - - - - - - - - - - - - - - 1
GUIDANCE ON EMC COMPATIBILITY - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2
INSTALLING THE HOSPIRA MEDNET
CONFIGURATION GUIDE - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4
G
ENERAL NOTES - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4
S
COPE - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4
A
SSUMPTIONS - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4
I
NTRODUCTION - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4
S
CREENS - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5
S
TATUS PROPERTIES SCREEN - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5
E
THERNET PROPERTIES - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6
W
IRELESS PROPERTIES - WIRELESS ENABLED - - - - - - - - - - - - - - - - - - - - - - - - 6
W
IRELESS ENABLED- DHCP ENABLED - - - - - - - - - - - - - - - - - - - - - - - - - - - 8
S
ECURITY - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -10
WEP - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11
WPA P
WPA E
WPA E
C
ERTIFICATES - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 15
HMSS (H
S
ERVICE - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -16
A
DMINISTRATION - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 17
F
INISH CONFIGURATION - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 17
WIRELESS LAN DEVICE SPECIFICATIONS - - - - - - - - - - - - - - - - - - - - - - - - - - - 18
EDERAL COMMUNICATIONS COMMISSION) STATEMENT - - - - - - - - - - - - - - 1
NTERFERENCE STATEMENT - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1
®
PLUG ’N PLAY MODULE (LIST 20677-04) - - - - - - - 3
To Replace the Module, proceed as follows: - - - - - - - - - - - - - - - - - - - - 3
ERSONAL - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12
NTERPRISE - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 13
NTERPRISE - AUTHENTICATION TYPE - - - - - - - - - - - - - - - - - - - - - - - - - 14
OSPIRA MEDNET
®
SERVER SUITE) - - - - - - - - - - - - - - - - - - - - - - - - - 16
CE Configuration Guide 430-11541-001
Introduction to the MedNet Wireless Module
The Hospira MedNet 802.11 a/b/g Wireless Upgrade Module is designed as an upgrade
module for Hospira Plum A+ Infusion Systems (Lists 20792, 20679, 12391 & 11791). The
host units are mobile infusion devices designed to be employed in the medical care environment. The wireless functionality afforded to the host units from the upgrade module
include the ability to download drug library information for simultaneously operating
hosts without requiring a physical connection and the time spent visiting the rooms they
occupy.
FCC Information
US FCC (Federal Communications Commission) Statement
• This device complies with part 15C, 15E of the FCC Rules. Operation is subject to
the following two conditions: (1) This device may not cause interference, and (2)
This device must accept any interference, including that may cause undesired
operation of these devices.
FCC Interference Statement
• This equipment has been tested and found to comply with the limits for a Class B
digital device, pursuant to Part 15C, 15E of the FCC Rules. These limits are designed
to provide reasonable protection against harmful interference in a residential
installation. This equipment generates, uses, and can radiate radio frequency energy.
If not installed and used in accordance with the instructions, it may cause harmful
interference to radio communications. However, there is no guarantee that
interference will not occur in a particular installation. If this equipment does cause
harmful interference to radio or television reception, which can be determined by
turning the equipment off and on, the user is encouraged to try and correct the
interference by one or more of the following measures:
- Reorient or relocate the receiving antenna.
- Increase the distance between the equipment and the receiver.
- Connect the equipment to an outlet on a circuit different from that to which the
receiver is connected.
- Consult the dealer or an experienced radio/TV technician for help.
• Changes or modifications not expressly approved by Hospira could void the user's
authority to operate the equipment.
Radio Frequency Exposure Statement
• The Wireless LAN radio device in the Connectivity Engine peripheral board with this
infusion device has been evaluated and found compliant to the requirements of the
following Radio Frequency exposure standards:
- Federal Communications Commission, OET Bulletin 65 (Edition 97-01),
Supplement C (Edition 01-01), Evaluating Compliance with FCC Guidelines for
Human Exposure to Radio frequency Electromagnetic Fields, July 2001.
CE Configuration Guide 1 430-11541-001
- Industry Canada, Evaluation Procedure for Mobile and Portable Radio
Transmitters with respect to Health Canada's Safety Code 6 for Exposure of
Humans to Radio Frequency Fields, Radio Standards Specification RSS-102
Issue 1 (Provisional): September 1999.
• The radiated output power of this Wireless LAN device is far below the FCC radio
frequency exposure limits. The Wireless LAN device has been evaluated with zero
inches separation of human body from the antenna and found to be compliant with
FCC RF exposure limits.
Guidance on EMC Compatibility
• There is a shared responsibility between manufacturers, customers and users to
ensure that Medical Equipment and Systems are designed and operated as intended.
Medical electrical equipment needs special precautions regarding electromagnetic
compatibility and needs to be installed and used according to the electromagnetic
compatibility information provided in this manual.
• The device is suitable for use in all establishments, including domestic
establishments. If extended operation during power mains interruption is needed, use
battery power.
• Always manage the electromagnetic environment.
• The guidance included in this manual provides information needed to:
- Determine the device’s suitability for use in the intended environment.
- Manage the electromagnetic environment to permit the device to perform as
intended without disturbing other equipment.
• Separate the device from all other electronic equipment. If the device must be used
near other electrical equipment, monitor the equipment to ensure there is no
electromagnetic interference.
• Devices should not be used adjacent to or stacked with other equipment. If the device
must be used adjacent to or stacked with other equipment, monitor the devices to
verify normal operation.
• USE ONLY components specifically labeled for use with the Plum A+ Infusion
System to help ensure the device operates as intended.
• If you suspect external RF sources or other equipment are influencing device
operation, contact the biomedical engineering department for additional guidelines
concerning electromagnetic immunity.
• Contact the biomedical engineering department for additional information in the
technical service manual concerning operating devices near RF sources.
• This device has been tested with the Hospira Plum A+ Infusion System and found to
comply with the International Standard IEC 60601-1-2 Edition 2.1 Electromagnetic
Compatibility (EMC) of Medical Electrical Equipment.
430-11541-001 2 CE Configuration Guide
Installing the Hospira MedNet® Plug ’n Play Module (List 20677-04)
Note: For use with Hospira Plum A+ Infusers with software version 10.3 and
higher.
Note: The recommended tool for this procedure is a No. 2 Phillips screwdriver.
CAUTION: CAUTION: Use proper ESD grounding techniques when handling
components. Wear an antistatic wrist strap and use an ESD-protected workstation.
Store the PWA in an antistatic bag before placing it on any surface.
To Replace the Module, proceed as follows:
1. Press [ON/OFF] to power the infuser
OFF.
2. Disconnect the infuser from AC
power.
CAUTION: Infuser must be
powered off for at least 2 minutes
prior to removing the module.
3. Carefully place the infuser face down.
4. Using a No. 2 Phillips screwdriver,
remove the two screws from the
module (one in the upper left corner
and one in the lower left corner). Refer
to Figure 1.
5. Carefully pull the module away from the infuser.
Figure 1. Remove Screws
Note: Note: When removing the module, note the placement guides the peripheral
PWA rests between.
6. Install the replacement module in the
exact reverse order of removal using
the screws and lock washers included
with the replacement module. Refer
to Figure 2.
Note: Note: Verify the module is
placed properly between the guides
and fits correctly into the CPU PWA.
7. Connect the infuser to AC power.
8. To verify successful module
replacement, power ON the infuser
and let the system perform its
self-tests. The screen will display an
E453 Malfunction.
9. Power the infuser OFF, and then ON
again.
10. If upgrading from version 12.x, The infuser is ready for operation.
11. If upgrading from version 10.x or 11.x:
a) Enter the serial number.
b) Power the infuser OFF, and then ON again. The infuser is ready for operation.
Figure 2. Insert Module
CE Configuration Guide 3 430-11541-001
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