SIMS Deltec CADD-PLUS 5400 User manual

i
Note: Colors are Black
and Cyan (as second color)
Model 5400
O perator’s Manual
Am bulatory Infusion Pum p
CADD-PLUS®
Deltec
SIM S D e lt e c, In c., St . Pau l , M N 5511 2 U .S.A.
This online version differs 
from the printed version.

Certain information that
is not intended for patients
has been removed.

ii
CADD, CADD-PLUS, Medication Cassette Reservoir and Medication Cassette Reservoir design are
SIMS trademarks
These products are covered by U. S. Patent Nos. 4,559,038; 4,565,542; 4,650,469 and D294,733;
other patents pending.
DURACELL®is a registered trademark of Duracell Inc. EVEREADY®ENERGIZER®is a regis-
tered trademark of Union Carbide Corp. ULTRALIFE®is a registered trademark of ULTRALIFE
Batteries, Inc.
This manual pertains only to the Deltec CADD-PLUS®, Model 5400, infusion pump.
The issue date of this Operator’s Manual is included for the clinician’s information.
In the event one year has elapsed between the issue date and product use, the clinician
should contact SIMS Deltec, Inc. to see if a later revision of this manual is available.
WARNING:
It is intended that this O perator’s Manual only be utilized by clinicians. Do not
permit patients to have access to this manual or otherwise disclose to the patient
the security code of the pump or any information w hich would allow the patient
to have complete access to all programming and operating functions.

iii
TECHNICAL ASSISTANCE
If you have comments or questions concerning the operation of the CADD-PLUS®
pump, please call this number: 800-426-2448.
Our staff is available to help clinicians twenty-four hours a day with the programming
and operation of the CADD-PLUS®infusion pump.
SIMS Deltec, Inc.
1265 Grey Fox Road
St. Paul, Minnesota 55112 U.S.A.

iv
CONTENTS
1.0 INTRODUCTION ................................................................................... 1
2.0 GENERAL DESCRIPTION OF CADD-PLUS®PUMP OPERATIONS .. 1
2.1 WARNINGS and CAUTIONS ....................................................... 2
2.1.1 WARNINGS ......................................................................... 2
2.1.2 CAUTIONS .......................................................................... 3
2.2 Physical Description of the Pump and Accessories ...................... 4
2.2.1 Items Packaged with the Pump ......................................... 5
2.2.2 Description of the Function Keys and Display Panel ......... 5
2.2.3 Description of the Reservoir or Administration Set ............ 6
2.3 Understanding the Delivery Modes .............................................. 7
2.4 Description of the Continuous Delivery Mode .............................. 7
2.4.1 The Reservoir-Residual Volume (RES VOL) .................... 7
2.4.2 Continuous Rate (ML/HR) ................................................. 8
2.4.3 The Amount GIVEN (GIVEN) ........................................... 8
2.5 Description of the Intermittent Delivery Mode ............................... 8
2.5.1 The Reservoir-Residual Volume (RES VOL) .................... 9
2.5.2 The Delivery Volume (ML) ................................................. 9
2.5.3 The Delivery PERIOD (PERIOD) ...................................... 9
2.5.4 The Delivery CYCLE (CYCLE) .......................................... 10
2.5.5 The KEEP VEIN OPEN (KVO) Rate ................................. 10
2.5.6 The DELAY START Function (DELAY START) ................ 10
2.5.7 The CYCLE GIVEN (CYCLE GIVEN) ............................... 11
2.5.8 The Amount GIVEN (GIVEN) ........................................... 11
3.0 OPERATOR INSTRCTIONS ................................................................. 12
3.1 Installing or Replacing the Battery ................................................ 13
3.2 Preparing to Program the CADD-PLUS®Pump ........................... 16
3.3 Programming the CADD-PLUS®Pump for Continuous Delivery .. 19
3.3.1 Selecting the Continuous Delivery Mode .......................... 19
3.3.2 Setting the Reservoir-Residual Volume (RES VOL) ......... 20
3.3.3 Setting the Continuous Delivery Rate (ML/HR) ................. 22
3.3.4 Reviewing the GIVEN Mode .............................................. 23
3.4 Programming the CADD-PLUS®Pump for Intermittent Delivery .. 24
3.4.1 Selecting the Intermittent Delivery Mode ........................... 24
3.4.2 Setting the Reservoir-Residual Volume (RES VOL) ......... 25
3.4.3 Setting the Delivery Volume (ML) ...................................... 27

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3.4.4 Setting the Delivery period (PERIOD) ............................... 28
3.4.5 Setting the Delivery CYCLE (CYCLE) ............................... 29
3.4.6 Setting the KEEP VEIN OPEN (KVO) Function ................ 29
3.4.7 Setting the DELAY START (DELAY START) .................... 30
3.4.8 Reviewing the CYCLE GIVEN Mode ................................. 30
3.4.9 Reviewing the GIVEN Mode .............................................. 31
3.5 Attaching and Removing the Cassette ......................................... 32
3.5.1 Removing a Used Cassette ............................................... 32
3.5.2 Attaching the Cassette ...................................................... 33
3.6 Priming the CADD-PLUS®Pump Tubing ...................................... 34
3.7 Programming the Patient Lock Levels (LL0, LL1, and LL2) ......... 35
3.8 Starting and Stopping the Pump .................................................. 38
3.9 Reviewing the CADD-PLUS®Programming Modes ..................... 39
4.0 REFERENCE SECTION ....................................................................... 40
4.1 Glossary ....................................................................................... 40
4.2 Pump Maintenance and Cleaning ................................................ 42
4.3 Equipment Exposure to Radiation or Magnetic Resonance
Imaging (MRI) ............................................................................... 42
4.4 Alarms and Troubleshooting Chart ............................................... 43
4.4.1 The Reservoir-Residual (RES VOL) Volume Alarm .......... 45
4.4.2 The High Pressure (HI P) Alarm ........................................ 45
4.5 Specifications (Nominal) ............................................................... 46
4.5.1 Continuous ........................................................................ 46
4.5.2 Intermittent ........................................................................ 46
4.5.3 General ............................................................................. 47
4.6 Limited Warranty .......................................................................... 48

vi

1
Description
1.0 INTRODUCTION
The Deltec CADD-PLUS®pump provides measured drug therapy to patients in
hospital or outpatient settings. Health care professionals should use this manual
to learn how to operate the pump.
The purpose of this manual is to familiarize you with the CADD-PLUS®pump’s
functions, which are described in Section 2; and to instruct you in how to use
those functions, which are outlined in detail in Section 3. Section 4 is a refer-
ence.
2.0 GENERAL DESCRIPTION OF CADD-PLUS®PUMP
OPERATIONS
The CADD-PLUS®Model 5400 ambulatory drug delivery pump is indicated for
intravenous, intra-arterial, or subcutaneous infusion (excluding insulin).
Therapy should always be overseen by a physician or a certified, licensed healthcare
professional. The patient should be instructed in using and troubleshooting the
pump.
The pump’s flexibility in programming allows it to be used in a variety of set-
tings, including the home. The clinician may program the pump in either of two
modes: the Continuous mode or the Intermittent mode. In the Continuous mode,
the pump delivers medication at a constant rate; in the Intermittent mode, it
delivers medication at regular, preset intervals.

Description
2
2.1 WARNINGS and CAUTIONS
Read this entire Operator’s Manual before operating the CADD-PLUS®ambulatory
infusion pump.
Failure to properly follow warnings, cautions, and instructions could result in death
or serious injury to the patient.
2.1.1 WARNINGS
•Do not use a pump that appears to have been damaged or tampered with, or is not
functioning properly.
•Use only drugs and solutions which are stable under delivery conditions experi-
enced during use in the pump. Observe warnings packaged with the Medication
Cassette™Reservoir or CADD®Administration Set.
•Do not use the pump in the presence of flammable anesthetics or explosive gases.
•The pump does not have an air-in-line alarm, an air entrapment mechanism, or an
upstream occlusion detector mechanism. Periodic visual inspection is therefore
recommended.
•Back-pressure or fluid resistance, which depends upon drug viscosity and catheter
size, may result in system delivery inaccuracies.
•Only the CADD®Extension Set with Anti-Siphon Valve must be used with this
pump; other extension sets will result in system delivery inaccuracies.
•This pump is capable of being set at a residual volume higher than the capacity of
the fluid container. The reservoir-residual volume value should be programmed to
reflect the actual volume of the medication being used.
•Avoid dropping the pump or hitting the pump against a hard surface, as this could
cause the cassette to become detached and the battery cover to become detached
or loose. If the cassette becomes detached, an uncontrolled flow of medication
from the fluid container or a reflux of blood may result, which could result in
death or serious injury to the patient. If the battery door becomes detached or
loose, the battery will not be properly secured; this may result in loss of power,
nondelivery of drug, and, depending on the type of drug being administered,
death or serious injury.
•If the pump is dropped or hit, inspect the pump to ensure that the cassette did not
become detached and the battery cover did not become dislodged. Inspection
should include closing the clamp on the tubing, detaching the pump and inspect-
ing the hinges, and checking the clips on the battery door to ensure they are not
broken. If there appears to be damage, the patient should be instructed to imme-
diately contact his or her health care provider, the pump should be taken out of
service, and Deltec’s Customer Service department should be contacted for return
authorization. If there appears to be no damage, reattach the cassette following
the instructions in the Operator’s Manual.

3
Description
•To prevent the uncontrolled flow of medication, use a CADD®Extension Set with
Anti-Siphon Valve, a CADD®Administration Set with integrated anti-siphon valve,
or a CADD®Administration Set with an attached Add On Anti-Siphon Valve.
•Use of a syringe with the CADD®Administration Set may result in UNDER-
DELIVERY of medication. Syringe function can be adversely affected by varia-
tions in plunger dimension and lubricity, which can result in greater force being
required to move the plunger. A syringe will lose plunger lubrication as it ages
and, as a result, the amount of under-delivery will increase which could, on occa-
sion, be significant. Therefore, the type of medication therapy and delivery accu-
racy required must be considered when using a syringe with the CADD®pump.
Clinicians must regularly compare the volume remaining in the syringe to the
pump’s displayed values such as RES VOL and GIVEN in order to determine
whether under-delivery of medication is occurring and, if necessary, take appro-
priate action.
2.1.2 CAUTIONS
•This device is not intended to be used for delivery of blood or cellular blood
products.
•This device may interfere with ECG equipment. Monitor ECG equipment care-
fully when using this device.
•The pump is not sterile. It is not designed to be sterilized. Sterilization could
damage the microcomputer and other pump parts.
•The pump should be routinely cleaned and kept free of dirt, liquids, and foreign
objects.
•Do not store the pump at temperatures below -40°C (-40°F ) or above 55°C
(131°F).
•Do not operate the pump at temperatures below +2°C (35°F) or above 40°C
(104°F).
•Do not expose the pump to humidity levels above 90% R. H.
•The pump is water resistant. However, total immersion is not recommended be-
cause moisture buildup within the case may damage the parts. Do not use pump
in the shower, sauna, or steam bath.
•Do not store the pump for prolonged periods with a battery; the battery could
leak and damage the pump.
•Avoid using the pump in close proximity to sources of strong static electricity or
strong electromagnetic fields.
•The use of a Deltec Pump Pouch is recommended. If the pump is dropped or
inadvertently hit against a hard surface, the pump pouch is designed to minimize
the need for servicing.

Description
4
2.2 Physical Description of the Pump and Accessories
The following diagram, Figure 1, illustrates the CADD-PLUS®pump and its
major functions.
Figure 1. The CADD-PLUS®pump.
STOP
START
LO K SELE T
MODE
SET
LEAR
STOP
GIVEN
LO BAT
RES VOL
ML/HR
DELAY
START
PERIOD
CYCLE
KVO HR MIN
CADD-PLUS
®
08/25/94 D. Zurn “PLUS w/4 callouts”
PRIME
Display (L D)
Keyboard
Scroll Keys
assette (the part of the
Medication assette™ Res-
ervoir or ADD® Adminis-
tration Set that attaches to
the pump)
®

5
Description
2.2.1 Items Packaged with the Pump
Packaged with the pump are the following items:
1 Battery (9-volt)
1 50 ml Medication Cassette™Reservoir (nonsterile, for demonstration
only)
1 Carrying case
1 Carrying pouch
1 Operator’s Manual with warranty information
The following products are also compatible with the CADD-PLUS®pump:
•Medication Cassette™Reservoir (50- or 100-ml), to be used with the
Extension Set with Anti-Siphon Valve
•CADD®Administration Set with integrated or Add On Anti-Siphon Valve
•Pump Pouches
2.2.2 Description of the Function Keys and Display Panel
Liquid Crystal Display (LCD). This is the pump’s display panel; the screen
which shows the pump’s various functions or modes and the values you pro-
gram for them. In this manual, the term “display”is synonymous with display
panel or LCD.
STO P/START Key. Press and hold the STOP/START key to start or stop pump
delivery.
SET/CLEAR Key. Use the SET/CLEAR key for programming, setting or reset-
ting, and clearing of numbers in the computer’s memory. You also use this key
for setting the Continuous or Intermittent mode.
PRIME Key. Use the PRIME key to fill the tubing and to remove air bubbles
from the fluid path.
LO CK Key. Use the LOCK key to lock out or limit the patient’s operation of the
pump.
SELECT MO DE Key. Use the SELECT MODE key to view the various delivery
and programming modes, such as Continuous or Intermittent delivery and RES
VOL. When the pump is in the Stop or Start mode, and you press and release the
SELECT MODE key, the pump will display each mode in succession. You will
have to press the SELECT MODE key each time you wish to access another
mode. (See Section 3.9, “Reviewing the CADD-PLUS®Programming Modes.”)
SCRO LL Keys. Use the up or down SCROLL keys to increase or decrease the
numeric value shown on the pump’s display.

Description
6
2.2.3 Description of the Medication Cassette™Reservoir or
CADD®Administration Set
The CADD-PLUS®pump may use a detachable Deltec, single use Medication
Cassette™Reservoir for holding the drug. They are available in 50 ml and
100 ml sizes.
A CADD®Administration Set may also be used to deliver medication from IV
bags of various sizes.
The procedures for attaching and removing the cassette (the part of the Medi-
cation Cassette™Reservoir or CADD®Administration Set that attaches to the
pump) are located in Section 3.
LOCKED
Figure 2. Discard a used Medication Cassette™Reservoir or CADD®
Administration Set immediately.
®

7
Description
2.3 Understanding the Delivery Modes
This section introduces the two delivery modes and their associated program-
ming modes that appear on the CADD-PLUS®pump display: (1) the Continu-
ous (C) delivery mode; and (2) the Intermittent (I) delivery mode. Further details
concerning these delivery modes are introduced in Section 3.3, “Programming
the CADD-PLUS®Pump for Continuous Delivery,”and Section 3.4, “Program-
ming the CADD-PLUS®Pump for Intermittent Delivery.”
2.4 Description of the Continuous Delivery Mode
Programming the pump in the Continuous delivery mode (Cmode) permits a
steady infusion rate. (See Figure 3.) In this mode, you can program the pump to
deliver medication at a constant rate in milliliters per hour.
Figure 3. The Continuous delivery mode.
2.4.1 The Reservoir-Residual Volume (RES VOL)
The reservoir-residual volume (RES VOL) refers to the initial amount of medi-
cation (in milliliters), contained in the fluid container, that you wish to deliver.
You must enter that amount into the computer’s memory to determine the amount
of medication remaining in the fluid container. [See Section 3.3.2, “Setting the
Reservoir-Residual Volume (RES VOL).”]
Delivery
Rate
(ML /H R )
Tim e (Continuous Delivery)

Description
8
2.4.2 Continuous Rate (ML/HR)
The delivery rate in ML/HR (milliliters per hour) is the constant rate at which
the pump delivers medication. The delivery rate range is from 00.1 ml/hr to 75.0
ml/hr in 00.1-ml/hr increments. If you program a delivery rate of 00.0 ml/hr,
delivery will not occur.
2.4.3 The Amount GIVEN (GIVEN)
GIVEN refers to the number of milliliters that have been delivered since the
GIVEN register was last cleared.
The number of milliliters in GIVEN accumulates from 000 to 999 and then
returns to 000. Please note that the GIVEN counter functions in a way that is
similar to an automobile’s odometer. After the GIVEN counter reaches 999, it
will start at 000 again and continue counting, which is especially important if
you plan to use more than 1,000 milliliters of solution.
2.5 Description of the Intermittent Delivery Mode
Programming the pump in the Intermittent delivery mode (I mode) permits the
infusion of a prescribed volume of drug (delivery volume) over a specified time
period (delivery PERIOD). You can repeat that program in a cycle of up to 24
hours (delivery CYCLE). When you are not infusing a drug dose, you may also
program the pump for a KEEP VEIN OPEN (KVO) function. The pump will
then deliver a minimal amount of a drug to maintain catheter patency. Finally,
you may also program the pump for a time delay (DELAY START) before
starting drug infusion. (See Figure 4.)

9
Description
2.5.1 The Reservoir-Residual Volume (RES VOL)
The reservoir-residual volume (RES VOL) refers to the initial amount of medi-
cation (in milliliters), contained in the fluid container, that you wish to deliver.
You must enter that amount into the computer’s memory to determine the amount
of medication remaining in the fluid container. [See Section 3.4.2, “Setting the
Reservoir-Residual Volume (RES VOL).”]
2.5.2 The Delivery Volume (ML)
The display will show the current delivery volume, which is the specific amount
of medication in milliliters that the pump will deliver during the PERIOD. The
delivery range is from 00.1 ml to 150.0 ml in 00.1 ml increments. If you pro-
gram a delivery volume of 0.00 ml, the pump will deliver medication at the
KVO rate.
2.5.3 The Delivery PERIOD (PERIOD)
You may program a specific amount of time, called the PERIOD, during which
the patient will receive a prescribed volume of a drug. (See Figure 4.) The display
will show the HR:MIN and PERIOD indicators that denote the current setting
for the PERIOD. The effective delivery rate (ML) during the PERIOD (HR:MIN)
may never exceed 75 ml/hr. The PERIOD range is from 10 minutes to 12 hours.
The PERIOD is programmable in 10-minute increments.
Figure 4. The Intermittent delivery mode.
DELAY
START
CYCLE
t0 t1 t2 t3
t0 to t1 = DEL AY STA RT
t1 to t2 = PER IO D
t1 to t3 = CY CL E
PERIOD
KVO
(option)
KVO
(option)
KVO
(option)
PERIOD
Tim e (HR : M IN )
Volum e
(ML )

Description
10
2.5.4 The Delivery CYCLE (CYCLE)
To repeat delivery of a preset volume (ML), it is necessary to program the pump
for a delivery CYCLE. (See Figure 4.) You will see the current CYCLE time in
hours and minutes on the display. You can program the CYCLE from 20 min-
utes to 12 hours and 10 minutes. The CYCLE is programmable in 10-minute
increments. The minimum amount of time for the CYCLE is the amount of time
programmed for the PERIOD plus 10 minutes. The special, 24-hour CYCLE
mode permits the delivery PERIOD to repeat once a day.
2.5.5 The KEEP VEIN OPEN (KVO) Rate
Setting the KVO rate is an optional function. Usually, you program the pump
for a KVO rate when you wish to deliver a minimal amount of drug to help
maintain catheter patency; consequently, you may use the KVO function be-
tween infusion periods and during the DELAY START. (See Figure 4.) The
KVO setting is active between each PERIOD and during the DELAY START
unless the KVO rate has been set at 00.0.
2.5.6 The DELAY START Function (DELAY START)
The DELAY START function, an optional feature, delays the start of a drug
delivery sequence. (See Figure 5.) The DELAY START function ranges from 10
minutes to 12 hours, and you can program it in 10-minute increments. If you
program the DELAY START function for “0”hours and “0”minutes, a delay
Figure 5. The DELAY START function.
DELAY START
(1 HR : 30 MIN)
CYCLE
4:30 PM
(N ow)
6:00 PM
(Begin CY CL E)

11
Description
will not occur, and the pump will begin its delivery immediately. For example,
if it is 4:30 pm, and you do not want the delivery of the drug to begin until 6:00
pm, you would program the DELAY START for 1HR:30MIN, which means
that the delivery would not begin until 6:00 pm.
2.5.7 The CYCLE GIVEN (CYCLE GIVEN)
CYCLE GIVEN shows the time that has elapsed since the last dose began.
CYCLE GIVEN is automatically set to 00:00 when the clinician programs a
new drug delivery profile or a new DELAY START time. When the pump is
started, CYCLE GIVEN waits until the DELAY START time, if any, passes.
Then it begins to count in 1-minute increments (or 1-hour increments in the 24-
hour mode) until it equals the programmed delivery CYCLE. At that point,
CYCLE GIVEN automatically resets to 00:00 and a new cycle begins.
If the pump is stopped at any time during the cycle, CYCLE GIVEN stops
counting. When the pump is restarted, CYCLE GIVEN resumes counting at the
same point in the cycle at which it was stopped.
NOTE:
If necessary, you can reset the CY CL E GIVEN in L L0 or L L1. To do this, display
the D EL AY START screen and press SET/CLEA R . Even if the D EL AY STA RT
is 00:00, the CY CL E G IVEN w ill clear to 00:00 and a new cycle w ill begin w hen
the pump is restarted.
2.5.8 The Amount GIVEN (GIVEN)
GIVEN refers to the number of milliliters that have been delivered since the
GIVEN register was last cleared.
The number of milliliters in GIVEN accumulates from 000 to 999 and then
returns to 000. Please note that the GIVEN counter functions in a way that is
similar to an automobile’s odometer. After the GIVEN counter reaches 999, it
will start at 000 again and continue counting, which is especially important if
you plan to use more than 1,000 milliliters of solution.

Operating Instructions
12
3.0 OPERATOR INSTRUCTIONS
This section describes how to operate the CADD-PLUS®pump. It contains de-
tailed, step-by-step instructions that will enable you to perform the following
tasks.
•Installing a battery and observing the Power-up Test ............ (Section 3.1)
•Preparing to program the pump ............................................... (Section 3.2)
•Programming the functions in the Continuous mode ............ (Section 3.3)
•Programming the functions in the Intermittent mode ............ (Section 3.4)
•Attaching the cassette ............................................................. (Section 3.5.2)
•Priming the tubing ..................................................................... (Section 3.6)
•Setting the lock levels (LL0, LL1, or LL2) ............................... (Section 3.7)
•Starting and stopping the pump ............................................... (Section 3.8)
•Reviewing the CADD-PLUS®programming modes ............... (Section 3.9)

Operating Instructions
13
3.1 Installing or Replacing the Battery
Use a new, 9-volt alkaline or lithium battery to power the pump. (See Section
4.5.3, “General Specifications,”for further information regarding batteries.)
WARNING:
•Do not use rechargeable NiCad or nickel metal hydride (NiMH) batteries. Do
not use carbon zinc (“heavy duty”) batteries. They do not provide sufficient
power for the pump to operate properly, which could result in death or serious
injury to the patient.
•Alw ays have new batteries available for replacement. If pow er is lost, nonde-
livery of drug, and, depending on the type of drug being administered, death or
serious injury to the patient could result.
•There is no pump alarm to alert users that the battery
has not been properly installed or has become dis-
lodged. An improperly installed or dislodged bat-
tery could result in loss of power and non-delivery of
drug and, depending on the drug being adminis-
tered, could result in death or serious injury to he
patient.
•If the pump is dropped or hit, the battery door or tabs may break. Do not use
the pump if the battery door or tabs are damaged because the batteries will not
be properly secured; this may result in loss of pow er, nondelivery of drug, and,
depending on the type of drug being administered, death or serious injury to the
patient.
If the pump is in Lock Level 1 or Lock Level 2 when you replace the battery, the
pump will remain in either the Intermittent mode or the Continuous mode,
whichever was active before the old battery was removed. (See Section 3.7 for
more information about the pump’s lock levels.)
If the pump is in Lock Level 0 when you install a battery, the display will pause
on “C”for Continuous mode, or “I”for Intermittent mode. To resume power-
up, you must confirm the mode (see step 6, below.)
As soon as you install the battery, the pump will be
on; there is no On/Off switch. In order to install or
replace a battery, be sure to place the pump in the
Stop mode. Then, follow these steps:
STEP 1: Push down and hold the battery door release
button while sliding the door off.
STEP 2: Remove the used battery.
11/04/96 D. Zurn
«Batt Compart Tabs 11/96»
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D. Zurn
«Open
Locking
Door
11/96»

Operating Instructions
14
STEP 3: Install the battery in the compartment (bot-
tom-end first).
NOTE:
Be sure to match the polarity m ark ings of the new
battery (+and –) w ith those on the battery compart-
ment. If you put the battery in backw ards, the display
panel w ill be blank, and you w ill not hear a beeping
sound.
Use a new, 9-volt alkaline or lithium battery to power
the pump. You may use any alkaline battery, including
DURACELL®Alkaline MN 1604 and EVEREADY®
ENERGIZER®Alkaline #522, for example; or, use
the ULTRALIFE®Lithium U9VL battery. You may
also use an external power source to run the pump.
STEP 4: Place the battery door halfway over the bat-
tery compartment and press the battery into the
compartment by pushing down on top of the door
with your thumb.
STEP 5: Slide the door closed. Ensure that the door is
latched by trying to remove the door without press-
ing the release button.
WARNING:
If a gap is present anyw here between the battery door and the pump housing,
the door is not properly latched. If the battery door becomes detached or loose,
the batteries will not be properly secured; this could result in loss of power, non-
delivery of drug, and, depending on the type of drug being administered, death
or serious injury to the patient.
If the pump is in LL1 or LL2, the power-up sequence will start and the pump
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«Remove Batt 11/96»
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«Match Batt 11/96»
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D. Zurn
Close
Locking
Door
11/96