Graham Field LUMISCOPE 1147 User manual
Blood Pressure Monitor
Automatic Wrist Type
Model 1147
Instruction Manual
Read this manual before operating your
Blood Pressure Monitor.
Save this manual for future use.
1147-INS-LAB-RevD19
1147-INS-LAB-RevD19 2
CONTENTS
SAFETY GUIDELINES—READ BEFORE USE ...................................... 3
INTENDED USE....................................................................................... 4
CONTRAINDICATIONS ...................................................................... 4
PRODUCT DESCRIPTION ...................................................................... 5
SYMBOLS KEY................................................................................... 5
ABOUT BLOOD PRESSURE ............................................................. 7
DEVICE OVERVIEW........................................................................... 9
DISPLAY OVERVIEW ......................................................................... 9
SETUP.................................................................................................... 10
BATTERY INSTALLATION ............................................................... 10
SETTING THE CLOCK ..................................................................... 10
OPERATION .......................................................................................... 11
OPERATION SAFETY ...................................................................... 11
OPERATION PREPARATION........................................................... 12
MEASUREMENT POSTURE ............................................................ 13
APPLYING THE CUFF...................................................................... 13
TAKING A MEASUREMENT............................................................. 14
MEMORY FUNCTION ....................................................................... 15
AVERAGE MODE ............................................................................. 15
MAINTENANCE..................................................................................... 16
CLEANING........................................................................................ 16
DISINFECTION (WHEN CLEANING PROCESS IS COMPLETE) ... 16
STORAGE......................................................................................... 16
TROUBLESHOOTING........................................................................... 17
PRODUCT SPECIFICATIONS............................................................... 18
LIMITED WARRANTY ........................................................................... 19
1147-INS-LAB-RevD19 3
SAFETY GUIDELINES—READ BEFORE USE
The safety statements presented in this chapter refer to the basic
safety information that the Blood Pressure Monitor (BPM) user shall
pay attention to and abide by. There are additional safety statements in
other chapters or sections, which may be the same as or similar to the
following, or specic to the operations. Please note the following special
statements, used throughout this manual, and their signicance:
WARNING: Indicates a potential hazard situation or unsafe
practice that, if not avoided, could result in death or serious
personal injury.
CAUTION: Indicates a potential hazard or unsafe practice that, if
not avoided, could result in minor or moderate personal injury.
sNOTICE: Indicates a potential hazard or unsafe practice that, if
not avoided, could result in product or property damage.
Info: Provides application recommendations or other useful information to
ensure that you get the most from your product.
WARNING: Important! Read and understand these instructions
before using the Blood Pressure Monitor. If you do not
understand any part of these warnings, cautions or instructions,
contact a healthcare professional for direction in the use of
this product. If the Blood Pressure Monitor is not properly
assembled and used, personal injury and damage to the Blood
Pressure Monitor could result.
WARNING: This product should not be used without proper
instruction from a healthcare professional.
WARNING: If components are damaged or missing, contact
your Graham-Field authorized distributor immediately. DO NOT
use substitute parts. Use only Lumiscope replacement parts.
Non-Lumiscope replacement parts could cause personal injury
and damage to the Blood Pressure Monitor.
WARNING: Cancer and Reproductive Harm -
www.p65warnings.ca.gov.
WARNING: GF Health Products, Inc. assumes no responsibility for
any damage or injury caused by improper assembly or use of this
product.
1147-INS-LAB-RevD19 4
INTENDED USE
This device is intended for the noninvasive measurement of systolic and
diastolic arterial blood pressure and pulse rate in adults. The device is
intended to be used by adults, at room temperature, with skin contact.
CONTRAINDICATIONS
WARNING: Do not use this appliance on infants, children, or
persons who cannot express their own intentions.
WARNING: Consult your physician before use during
pregnancy.
WARNING: Consult your physician before use if diagnosed
with arrhythmia, arteriosclerosis, cardiovascular disease (such
as atherosclerosis), diabetes, liver or kidney disease, severe
hypertension, or peripheral circulatory disorders, etc.
1147-INS-LAB-RevD19 5
PRODUCT DESCRIPTION
SYMBOLS KEY
SYS
DIA
SN
IP20
Systolic Pressure
Diastolic Pressure
Direct Current
Type BF Applied Part
Attention, consult accompanying documents
Manufacturer
Serial Number
Irregular Pulse Detection
Keep dry
Do not dispose of the device or batteries with
household waste.
Follow operating instructions
Pumping
Pumping failure
Excessive body movement detected during
measurement.
SYS and DIA readings detected are not reasonable.
Cuff pressure is over 300 mmHg.
Insufficient pulse detected for measurement.
Temperature Limit
Humidity Limitation
Battery recycling symbol
Restriction of Hazardous Substances
REACH symbol- Registration, Evaluation,
Authorisation and Restriction of Chemicals (REACH)
is a European Union regulation.
Power "ON" / "OFF"
Protection against solid foreign objects > 12.5mm Ø
and no water-proof test
Pulse pressure is equal to systolic minus diastolic
1147-INS-LAB-RevD19 6
Symbols Key continued
SYS
DIA
SN
IP20
Systolic Pressure
Diastolic Pressure
Direct Current
Type BF Applied Part
Attention, consult accompanying documents
Manufacturer
Serial Number
Irregular Pulse Detection
Keep dry
Do not dispose of the device or batteries with
household waste.
Follow operating instructions
Pumping
Pumping failure
Excessive body movement detected during
measurement.
SYS and DIA readings detected are not reasonable.
Cuff pressure is over 300 mmHg.
Insufficient pulse detected for measurement.
Temperature Limit
Humidity Limitation
Battery recycling symbol
Restriction of Hazardous Substances
REACH symbol- Registration, Evaluation,
Authorisation and Restriction of Chemicals (REACH
)
is a European Union regulation.
Power "ON" / "OFF"
Protection against solid foreign objects > 12.5mm Ø
and no water-proof test
Pulse pressure is equal to systolic minus diastolic
1147-INS-LAB-RevD19 7
ABOUT BLOOD PRESSURE
What is blood pressure?
Blood pressure is the pressure produced by the force of blood owing
against artery walls after the heart ejects blood into the vessel system.
Systolic and diastolic pressures
Systolic pressure represents the highest pressure during heart
contraction and diastolic pressure is the lowest pressure while heart is
resting.
WHO / ISH classication
Your blood pressure measurement can be compared with classication
categories dened by 1999 World Health Organization – International
Society of Hypertension Guidelines for Management of Hypertension for
preliminary evaluation. Consult your physician for interpretation of blood
pressure measurement and follow their directions.
1147-INS-LAB-RevD19 8
Blood pressure uctuation and variation
Human blood pressure uctuates and will vary 24 hours a day. Blood
pressure measurement can be affected by the measurement position,
posture, and physiologic condition as well as factors such as eating,
bathing, exercising, smoking, drinking alcohol, stress, mental tension,
breathing, conversation, movement, temperature or humidity change,
etc.
Obtaining reliable measurements
In order to obtain reliable measurements, follow recommendations
below:
1. Keep taking and recording blood pressure measurement consistently
at the same time every day to establish your blood pressure pattern.
2. Wait at least thirty minutes after eating, bathing, smoking, exercising,
or ingesting caffeine or alcohol before measurement.
3. Remove constricting clothing or ornaments from your arm and
ensure the range of cuff circumference is applicable to you.
4. Be seated and relax for at least ve minutes in a quiet and
comfortable place prior to measurement.
5. Wait at least ve minutes between measurements, so that your blood
vessels can return to the state they were in before measurement.
Rest between repeated measurements.
1147-INS-LAB-RevD19 9
DEVICE OVERVIEW
Info: This product includes one blood pressure monitor, one
cuff, one instruction manual, three AAA alkaline batteries, and
one storage bag / case.
DISPLAY OVERVIEW
1147-INS-LAB-RevD19 10
SETUP
BATTERY INSTALLATION
1. Remove the battery cover and insert batteries into the battery
compartment with polarities “+” and “-” matching polarity indicator.
Replace the battery cover.
2. Use only fully-charged AAA alkaline batteries.
3. Always replace all three batteries at the same time.
4. The built-in clock may need to be reset and reading memories may
be erased after battery replacement.
5. Dispose of used batteries in compliance with local regulations for
environmental protection.
SETTING THE CLOCK
1. To have correct date and time for memory storage, the built-in clock
needs to be set before beginning rst measurement.
2. Under power-off mode, press and hold the MEMORY button until
the display shows a blinking year, then press the POWER button for
adjustment. After current year is selected, press the MEMORY button
to set it and switch to next adjustment.
3. Repeat previous steps to adjust and set current month, day, hour,
and minute one by one while they are blinking.
4. AFTER setting the clock, proceed to step 5 to nish setting the clock,
or press the MEMORY button if you wish to set the ALARM feature.
a. Press the POWER button until the desired time is shown.
b. Press the MEMORY button to save desired time for AL1 (user 1).
c. Proceed to step 5 to nish setting the clock, or press the
MEMORY button to set the ALARM feature for the next user; you
may continue in this manner to set the ALARM for users 2, 3 and
4 (AL2, AL3, and AL4).
5. Press the MEMORY button again to nish setting the clock.
1147-INS-LAB-RevD19 11
OPERATION
OPERATION SAFETY
sNOTICE: The unit is not waterproof. Do not immerse this
instrument in liquid.
WARNING: Read and follow the entire instruction manual before
operating this blood pressure monitor.
WARNING: Do not press the POWER button if the cuff has not
been properly applied.
WARNING: Do not use the instrument if you think it is damaged
or if you notice anything unusual.
WARNING: Do not disassemble or modify the device or cuff.
WARNING: Discard old batteries carefully, out of reach of
children. Swallowing the battery may be fatal. If the battery or
other small parts are swallowed, contact a hospital immediately
to have it removed.
WARNING: Avoid prolonged over-ination of the bladder to
prevent physical injury.
WARNING: If the cuff causes any discomfort during
measurement, press the POWER button to turn off the device
immediately.
WARNING: Keep blood pressure monitor away from children.
WARNING: This manual and the product are not substitutes
for visiting the physician. Neither the information contained
herein nor this product may be used to diagnose or treat health
problems, or to prescribe drugs. If you have or suspect that
you have a medical problem, seek immediate advice from your
physician.
WARNING: Measuring too frequently may result in circulatory
disorders, which can cause unpleasant sensations such as
localised bleeding under the skin or temporary numbness in
your arm. These symptoms do not usually last long; however, if
you have not recovered quickly, consult your physician.
1147-INS-LAB-RevD19 12
WARNING: Take into consideration the electromagnetic
compatibility of the unit (e.g. disruptions to the power supply,
radio frequency interference, etc.) Only use the unit indoors.
To avoid inaccurate results due to electromagnetic interference
between electrical and electronic equipment, do not use the unit
near mobile phones or microwave ovens. Keep devices whose
maximum power exceeds 2 W at least 11 feet (3.3 meters) from
the blood pressure monitor.
WARNING: Verify the accuracy of the blood pressure monitor
every two years. Contact an authorized agent or laboratory for
inspection / calibration service.
OPERATION PREPARATION
1. Do not conduct any measurements if the temperature is low (below
41°F / 5°C) or high (over 104°F / 40°C), or if the relative humidity
is beyond the range of 15% to 90%, as this can lead to inaccurate
readings.
2. Take the measurement at room temperature in a quiet and stress-
free environment.
3. Do not move yourself or the unit during the measurement. Do not
speak during the measurement.
4. Blood pressure varies naturally depending on the time of day and is
affected by many factors. Blood pressure is usually highest at work
and reaches its lowest level during sleep.
5. Blood pressure measurements should be assessed by a physician
or trained healthcare professional who is familiar with your medical
history. If you use the unit and regularly record the results, keep your
physician informed of any changes in your blood pressure.
6. The performance of this device can be affected as severe
arrhythmias such as atrial or ventricular premature beats or atrial
brillation are presented during measurement.
7. The blood pressure measurements conducted with this unit are
equivalent to measurements obtained by a trained observer in
accordance with the values achieved using the cuff/stethoscope
auscultation method and are within the specied EN 1060-4 standard
limits.
1147-INS-LAB-RevD19 13
MEASUREMENT POSTURE
1. Wait at least thirty minutes after nishing a caffeinated drink or
cigarette before measurement.
2. Sit down and relax for at least ve minutes before measurement.
3. Wait at least ve minutes between repeated measurements.
4. Use the same arm consistently for each measurement (preferably
the left) and take the measurement at about the same time every
day.
5. Sit down in a chair in a comfortable position with your elbows placed
on a table and both feet on the ground. Do not interlock your legs
during the measurement.
6. Sit with your hand relaxed, your arm extended in front of you and
palm facing up.
7. Sit upright in a chair with your feet at on the oor in a natural
position and relax.
APPLYING THE CUFF
1. Ensure your wrist circumference is within applicable cuff range.
2. Attach the cuff around your bare-skinned left wrist through the cuff
with with the display aligned with your palm. If it is not possible to
take measurement with the left arm, use the right arm instead.
3. Fasten the cuff with its bottom edge approximately 5/8inch (1 ~ 2 cm)
above your palm line. Ensure the cuff is not wrapped too tightly.
4. Sit upright in a chair with your feet at on the oor in a natural,
comfortable position and relax.
5. Steadily rest your forearm on a table with the cuff at heart level.
1147-INS-LAB-RevD19 14
TAKING A MEASUREMENT
Info: Remain still and do not talk during measurement.
1. Press the USER button to choose user number for memory storage.
User selection can also be made by pressing the USER button while
readings are displayed after measurement is completed.
2. Press the POWER button to start automatic measurement. The
measurement can be interrupted anytime by pressing the POWER
button again.
3. When the measurement is completed, the systolic pressure, diastolic
pressure and pulse rate will be displayed.
4. The display will indicate which category your blood pressure reading
belongs to according to classication dened in 1999 WHO / ISH
Guidelines for Management of Hypertension. Optimal and normal
categories are indicated with 1 or 2 bars from the bottom which fall
within the green indication, high-normal is indicated with the 3rd bar
from the bottom which falls within the yellow indication, and grade
1-3 hypertension categories are indicated with 4-6 bars from the
bottom which fall within the red indication.
5. IPD (Irregular Pulse Detection): The device can detect irregular pulse
(a pulse interval longer than 5/3 times the average pulse interval)
during measurement. The IPD indicator will appear when more than
three irregular pulses were detected during measurement. If the IPD
indicator is displayed with measurement readings frequently, consult
a physician for further directions.
6. The device also provides the PP (Pulse Pressure) function that is
equal to systolic minus diastolic. If systolic is higher than diastolic 60
mmHg, LCD will display “PP” and differentiation value. If PP indicator
is displayed with measurement readings frequently, please consult a
qualied physician for further direction.
7. Press the POWER button to turn off the device or it will turn off
automatically after 150 seconds non-operation. Readings will be
saved into memory automatically while powering off.
1147-INS-LAB-RevD19 15
MEMORY FUNCTION
1. Press the USER button to select desired user number for recalling
memories.
2. Press the MEMORY button to recall the last reading stored in the
memory.
3. Press the MEMORY button repeatedly to recall the next set of
previous readings.
4. To delete the current displayed readings from memory, press and
hold the POWER button until the display shows “dEL”, then press the
POWER button again; the current displayed reading is deleted after
three beeps are heard.
Info: The number displayed in front of “dEL” indicates which user’s
memory set is selected for deletion.
5. To erase all readings in memory, press and hold the POWER button
under memory mode until the display shows “dEL” and press the
MEMORY button to show “dEL ALL” on the display, then press the
POWER button; all readings in memory are erased after three beeps
are heard.
6. Press the POWER button to exit memory function.
AVERAGE MODE
Info: To select a specic user to average, select the user number rst by
pressing the USER button.
1. Press and hold the USER button for at least 3 seconds in STANDBY
status until “-L03” appears.
2. Press the USER button to switch between the average of the latest 3
readings (-L03), last 7 days (-d07), last 14 days (-d14), last 21 days
(-d21) and last 28 days (-d28).
3. Press the MEMORY button to switch between the morning, evening,
and all day average value. Press the USER button again to switch
between different period modes (last 3, morning, evening, or all day).
4. Press the POWER button to exit AVERAGE mode.
1147-INS-LAB-RevD19 16
MAINTENANCE
WARNING: Do not disassemble or modify the device or cuff.
sNOTICE: Do not drop the device. It is not shock proof.
sNOTICE: Do not twist the cuff.
sNOTICE: Do not store the device and cuff in direct sunlight, high
temperature, moisture, or severe dust.
sNOTICE: Do not use thinner, benzene, or other harsh cleaners
to clean the device.
sNOTICE: Do not wash or immerse any part of the device.
sNOTICE: Remove all batteries if the device is not likely to be
used for a long period of time.
CLEANING
1. Moisten a clean, soft cloth with a solution of 5-10% mild detergent to
clean water. Gently wipe the device with a contact time of at least 10
minutes.
2. Use a clean cloth moistened with clear, cool water to remove any
chemical residues remaining on the device.
3. If necessary, repeat steps 1 and 2 to ensure the device is clean.
4. Wipe dry with a clean, soft, cloth to avoid water stains.
DISINFECTION (WHEN CLEANING PROCESS IS COMPLETE)
1. Use 70 to 75% isopropyl alcohol in a spray bottle and spray both
sides of the cuff with it, with a contact time at least 10 minutes.
2. Use a clean cloth moistened with clear, cool water to remove any
chemical residue remaining on the device.
3. Air dry the device and cuff at a room temperature of 68°F ~ 86°F
(20°C ~ 30°C) for 3 ~ 4 hours.
STORAGE
sNOTICE: When the device is often in use, store it in a dry,
clean, and dust-free environment at a moderate temperature of
41°F ~ 104°F (5°C ~ 40°C), 15~90% RH. If the device is not likely
to be used for a long period of time, store it at a temperature of
-4°F ~ 131°F (-20°C ~ 55°C), < 93 % RH.
sNOTICE: Remove all batteries if the device is not likely to be
used for a long period of time.
1147-INS-LAB-RevD19 17
TROUBLESHOOTING
Pumping failure. Ensure the cuff’s bottom edge is
approximately 5/8inch (1 ~ 2 cm) above your palm line and
not wrapped too tightly.
Refasten the cuff and measure again.
Excessive body movement detected during measurement.
Refasten the cuff and measure again.
Insufcient pulse detected for measurement.
Refasten the cuff and measure again.
Detected SYS and DIA readings are not reasonable,
possibly as a result of too much interference. Keep the unit
away from mobile phones and microwave ovens.
Refasten the cuff and measure again
The pumping pressure is over 300 mmHg. The cuff may be
improperly wrapped.
Refasten the cuff and measure again.
Replace all batteries.
1147-INS-LAB-RevD19 18
PRODUCT SPECIFICATIONS
Measuring Range Pressure: 20 ~ 300 mmHg
Pulse Rate: 40 ~ 200 pulse/min.
Accuracy Pressure: ± 3 mmHg
Pulse Rate: ± 5 % of reading
Measuring Method Oscillometric method
Ination Method Electrical rolling pump
Deation Method Mechanical release valve
Rapid Exhaust Electrical solenoid valve
Display Digital LCD (Liquid Crystal Display)
Memory 2 x 50 sets
Operation Condition 41°F - 104°F (5°C ~ 40°C), 15 ~ 90 % RH
Storage Condition -4°F ~ 131°F (-20°C ~ 55°C), < 93 % RH
IP Classication
IP20 (Protection against touching foreign bodies
<.5 in. (12.5 mm) and no water-proof test)
Power Source Two AAA alkaline batteries (included)
Battery Life ~ 250 measurements with alkaline batteries
Power Saving Auto-off after 150 sec. non-operation
Size 3.3 in. x 2.9 in. x 1.4 in.
(83 mm x 74 mm x 35 mm)
Weight ~ 5.29 oz. (150 g) including batteries
Cuff Range 5.31 in. ~ 8.66 in. (13.5 cm ~ 22 cm)
1. This blood pressure monitor is designed to comply with requirements of European Standard
EN ISO 81060-1:2012 Non-invasive sphygmomanometers - Part 1: Requirements and test
methods for non-automated measurement type, EN 1060, Noninvasive sphygmomanometers
- Part 3: Supplementary requirements for electro-mechanical blood pressure measuring
systems.
2. Blood pressure measurements determined with this device are equivalent to those obtained
by a trained observer using the cuff/stethoscope auscultatory method, within the limits
prescribed by the American National Standard ANSI/AAMI SP10, “Manual, electronic, or
automated sphygmomanometers.”or automated sphygmomanometers.”
1147-INS-LAB-RevD19 19
LIMITED WARRANTY
SCOPE OF WARRANTY
GF Health Products, Inc. (“GF”) warrants to the original purchaser only that it will replace or repair
components, at GF’s sole discretion, that are defective in material or workmanship under normal use and
service. All warranties are conditioned upon the proper use of the products strictly in accordance with good
commercial practice and applicable GF instructions and manuals, including proper use and maintenance.
To the extent that a component is warranted by a third party, GF conveys all of its rights under that
warranty to the original purchaser, to the extent permitted. This limited warranty shall only apply to defects
that are reported to GF’s customer service team within the applicable warranty period and which, upon
examination by GF or its authorized representative, prove to be a warranty item. This limited warranty is
not transferable. Within the guidelines set forth in this document, this product is warranted for one (1) year.
The applicable warranty period shall commence from date of shipment to the original customer, unless
there is an expiration date on the component in which case the warranty shall expire on the earlier of
warranty period or the expiration date.
OBTAINING WARRANTY SERVICE
This limited warranty shall only apply to defects that are reported to the Distributor from whom the
Customer purchased the product within the applicable warranty period. If there is not a Distributor, you
must contact GF directly by calling 1.770.368.4700, sending a fax request to 1.770.368.2386, or by
e-mailing a request to cs@grahameld.com. Specic directions will be provided by the Customer Service
Representative. Failure to abide by the specic directions will result in denial of the warranty claim.
EXCLUSIONS
The warranty does not cover and GF shall not be liable for the following:
1) Defects, damage, or other conditions caused, in whole or in part, by misuse, abuse, negligence,
alteration, accident, freight damage, tampering or failure to seek and obtain repair or replacement in a
timely manner;
2) Products which are not installed, used, or properly cleaned and maintained as required in the ofcial
manual for the applicable product;
3) Products considered to be of a non-durable nature including, but not limited to: batteries, accessories,
casters, lters, fuses, gaskets, lubricants, and charts;
4) Accessories or parts not provided by GF;
5) Charges by anyone for adjustments, repairs, replacement parts, installation or other work performed
upon or in connection with such products which are not expressly authorized in writing, in advance, by
GF;
6) Any labor or shipping charges incurred in the replacement part installation or repair;
7) Costs and expenses of regular maintenance and cleaning; and
8) Representations and warranties made by any person or entity other than GF.
ENTIRE WARRANTY, EXCLUSIVE REMEDY AND CONSEQUENTIAL DAMAGES DISCLAIMER
THIS WARRANTY IS GF’S ONLY WARRANTY AND IS IN LIEU OF ALL OTHER WARRANTIES,
EXPRESS OR IMPLIED. GF MAKES NO IMPLIED WARRANTIES OF ANY KIND INCLUDING ANY
IMPLIED WARRANTIES OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. IF
ANY MODEL OR SAMPLE WAS SHOWN TO THE CUSTOMER, SUCH MODEL OR SAMPLE WAS
USED MERELY TO ILLUSTRATE THE GENERAL TYPE AND QUALITY OF THE PRODUCT AND NOT
TO REPRESENT THAT THE PRODUCT WOULD NECESSARILY CONFORM TO THE MODEL OR
SAMPLE IN ALL RESPECTS. THIS WARRANTY IS LIMITED TO THE REPAIR OR REPLACEMENT OF
THE DEFECTIVE PARTS. GF SHALL NOT BE LIABLE FOR AND HEREBY DISCLAIMS ANY DIRECT,
SPECIAL, INDIRECT, INCIDENTAL, EXEMPLARY OR CONSEQUENTIAL DAMAGES, INCLUDING, BUT
NOT LIMITED TO: DAMAGES FOR LOSS OF PROFITS OR INCOME, LOSS OF USE, DOWNTIME,
COVER, OR EMPLOYEE OR INDEPENDENT CONTRACTOR WAGES, PAYMENTS AND BENEFITS.
The warranties contained herein contain all the representations and warranties with respect to the subject
matter of this document, and supersede all prior negotiations, agreements and understandings with
respect thereto. The recipient of this document hereby acknowledges and represents that it has not relied
on any representation, assertion, guarantee, warranty, collateral contract or other assurance, except
those set out in this document. For additional information on this product or this warranty, contact a GF
Customer Service Representative.
NOTES:
1) Additional terms and conditions may apply.
2) Freight claims must be notated on the appropriate shipping documents and must be made with
immediacy. International, federal and state regulations govern specic requirements for freight claims.
Failure to abide by those regulations may result in a denial of the freight claim. GF will assist you in
ling the freight claim.
3) Claims for any short shipment must be made within three (3) days of the invoice date.
1.770.368.4700
Information contained herein is subject to change.
The most current and complete product information can be found
on our website.
www.grahameld.com
© 2009, GF Health Products, Inc. All Rights Reserved.
Lumiscope is a trademark of GF Health Products, Inc.,
One Graham-Field Way, Atlanta GA 30340-3140
GF Health Products, Inc. is an ISO 13485 Certied Company.
Manufactured for GF Health Products, Inc.
Made in China
Table of contents
Other Graham Field Blood Pressure Monitor manuals
