Aneroid Sphygmomanometer
Use, Care, & Maintenance
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Device Description and Intended Use
LATEX
°
F
An aneroid sphygmomanometer is used by professional healthcare providers and
individuals trained in the auscultatory blood pressure technique to determine systolic
and diastolic blood pressure in humans.
Cuff Size
Contraindications:
Aneroid sphygmomanometers are contraindicated for neonate use. Do not
use with neonatal cuffs or neonate patients. Review the size chart (right) for
proper limb range usage.
Infant 7I 3.5 to 5.5 9 to 14
Child 9C 5.1 to 7.6 13 to 19.5
Small Adult 10SA 7.4 to 10.6 19 to 27
Adult 11A 9 to 15.7 23 to 40
Large Adult 12X 13.3 to 19.6 34 to 50
Thigh 13T 15.7 to 25.9 40 to 66
Symbol Definitions
The following symbols are associated with your aneroid sphygmomanometer.
Symbol Definition
Not made with natural
rubber latex
Important Warning/Caution
Circumference Size
Conforms to EU Standards
Symbol Definition
Represenative’s Information
Manufacturer’s Information
Temperature Limit
Humidity Limitation
Limb Range
Inches CM
Authorized European
Size Chart
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General Warnings
!
A warning statement in this manual identifies a condition or practice
which, if not corrected or discontinued immediately could lead to patient
injury, illness, or death.
WARNING:
!
Do not allow a blood pressure cuff to remain on patient for more than
10 minutes when inflated above 10 mmHg. This may cause patient distress, disturb blood circulation, and contribute to the injury of peripheral nerves.
!
WARNING:
If luer lock connectors are used in the construction of tubing, there is
a possibility that they might be inadvertently connected to intra-vascular fluid systems, allowing air to be pumped into a blood vessel. Immediately consult a physician if
this occurs.
!
WARNING: Safety and effectiveness with neonate cuff sizes 1 through 5 is not
established.
WARNING: If this equipment is modified, appropriate inspection and testing
!
must be conducted to ensure its continued safe use.
WARNING: Do not apply cuff to delicate or damaged skin. Check cuff site fre-
!
quently for irritation.
WARNING: Only use the cuff when the range markings indicated on the cuff
!
show that the proper cuff size is selected, otherwise erroneous readings may result.
WARNING: Allow space between patient and cuff. Two fingers should fit in this
!
space if the cuff is correctly positioned.
WARNING: Do not apply cuff to limbs used for IV infusion.
!
WARNING: Patient should remain still during measurement to avoid erroneous
!
readings.
!
WARNING: When using with an infant or child cuff, extra care must be taken to
prevent over-inflation. With smaller cuffs (infant or child) the cuff can inflate to
over 300mmHg with just two full compressions of the bulb. To prevent discomfort
or injury to the patient and damage to the instrument, bulb should only be partially
squeezed, so that each “stroke” inflates the cuff in 40mmHg to 60mmHg increments
until inflated to the desired level.
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!
WARNING: This product may contain a chemical known to the state of California
to cause cancer, birth defects, or other reproductive harm.
!
CAUTION:
To obtain the greatest accuracy from your blood pressure instrument,
it is recommended that the instrument be used within a temperature range of 50°F
(10°C) to 104°F (40°C), with a relative humidity range of 15%-85% (non-condensing).
!
CAUTION: Extreme altitudes may affect blood pressure readings. Your device has
been designed for normal environmental conditions.
Operation of Pocket Aneroids
This booklet contains operating and main-
Hang
Tab
tenance information for pocket aneroid
sphygmomanometers. Please read and retain.
Your pocket aneroid sphygmo-
Gauge
manometer consists of an aneroid
manometer (gauge), complete inflation system, (latex-free inflation bladder, squeeze bulb, and the valve), a
zippered carrying case, and operating
Artery Mark
Bladder &
Tubing
instructions.
Most models come preassembled and ready for use. If assembly is required, attach
gauge and bulb and valve assemblies to the tubes as shown in illustration. To facilitate,
use alcohol or soapy water.
Cuff
Bulb & Valve
Index Line
Measurement Procedure
1. Patient Position
The patient should sit or lie comfortably. The arm should be fully supported on a flat
surface at heart level. (If the arm’s position varies, or is not level with the heart, measurement values obtained will not be consistent with the patient’s true blood pressure.)
When seated, the patient should have their back and arm supported, and their legs should
not be crossed. The patient should relax prior to measurement comfortably for five (5)
minutes and should refrain from talking or moving during measurement. Observer
should view manometer in a direct line to avoid “Parallax error”.
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2. Apply the cuff
Range
CORRECT
Select Smaller Cuff
Select Larger Cuff
Nylon cuffs are specially designed to promote
Left Arm
the precisely accurate determination of blood
pressure. Index and range markings ensure
use of the correct cuff size. The artery mark
indicates proper cuff positioning.
Place the cuff over the bare upper arm with
Tube
(Figure 1)
the artery mark positioned directly over the
brachial artery. The bottom edge of the cuff should be positioned approximately (1”)
one inch (2-3cm) above the antecubital fold. Wrap the end of the cuff not containing the
bladder around the arm snugly and smoothly and engage adhesive strips (Figure 1).
NOTE: If the unit is equipped
with a calibrated nylon cuff,
featuring Index and Range
markings, a correct fit may be
verified by checking that the
Index Line falls between the
two Range Lines. (Figure 2).
3. Inflate the cuff
Index Lines
Close the valve by turning thumbscrew clockwise.
(Figure 2)
Range Lines
Palpate the radial artery while inflating the cuff. Be sure to inflate cuff quickly by
squeezing bulb rapidly.
Inflate cuff 20-30 mmHg above the point at which the radial pulse disappears.
NOTE: Cuff pressure range is 0 mmHg to 300 mmHg.
4. Position the Stethoscope
Position the chestpiece in the antecubital space below the cuff, distal to the brachium.
Do not place chestpiece underneath the cuff, as this impedes accurate measurement.
Use the bell side of a combination stethoscope for clearest detection of the low pitched
Korotkoff (pulse) sounds.
5. Deflate the cuff
Open the valve to deflate the cuff gradually at a rate of 2-3 mmHg per second.
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6. Measurement
Record the onset of Korotkoff sounds as the systolic pressure, and the disappearance of
these sounds as diastolic pressure. (Some healthcare professionals recommend recording diastolic 1 and diastolic 2. Diastolic one occurs at phase 4).
NOTE: It is recommended that K4 be used in children aged 3 to 12, and K5 should be
used for pregnant female patients unless sounds are audible with the cuff deflated, in
which case K4 should be used. K5 should be used for all other adult patients.
After measurement is completed, open valve fully to release any remaining air in the cuff.
Remove cuff.
Care and Maintenance
STORAGE:
Pocket Gauge: After measurement, fully exhaust cuff then wrap cuff around gauge and
bulb and store in zippered carrying case.
NOTE: This product will maintain the safety and performance characteristics
specified at temperatures ranging from 50°F to 104°F (10°C to 40°C) at a relative
humidity level of 15% to 85%.
This device can be safely stored at temperatures ranging from -4°F (-20°C) to 131°F
(55°C) with a relative humidity of 90%.
Manometer: Your pocket aneroid gauge requires minimal care and maintenance.
The manometer may be cleaned with a soft cloth but
should not be dismantled under any circumstances.
Gauge accuracy can be checked visually; simply be
certain the needle rests within the printed oval when the
unit is fully deflated (Figure 3).
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NOTE: Store gauge with
valve in full exhaust position.
(Figure 3)
Should the indicator needle of the manometer rest outside of this calibration mark,
then the manometer must be re-calibrated to within ±3 mmHg when compared to a reference device that has been certified to national or international measurement standards. A manometer whose indicator needle is resting outside of this mark, is NOT
acceptable for use.
In the event that the gauge is ever in need of calibration, simply return for service.
Damaged or broken parts will be replaced as needed at a minimal charge. Refer to the
warranty for specific details of warranty coverage.
The manufacturer recommends a calibration check every 2 years.
Cuff Cleaning and Disinfecting
NOTE: Use one or more of the following methods and allow to air dry:
• Wipe with mild detergent and water solution (1:9 solution). Rinse.
• Wipe with Enzol per manufacturer’s instructions. Rinse.
• Wipe with .5% bleach and water solution. Rinse.
• Wipe with 70% isopropyl alcohol.
• Launder with mild detergent in warm water, normal wash cycle.
Remove bladder first. Cuff is compatible with 5 wash cycles.
Low Level Disinfection
Prepare Enzol enzymatic detergent according to the manufacturer’s instructions. Spray
detergent solution liberally onto cuff and use a sterile brush to agitate the detergent solution over entire cuff surface for five minutes. Rinse continuously with distilled water
for five minutes. To disinfect, first follow the cleaning steps above, then spray cuff with
10% bleach solution until saturated, agitate with a sterile brush over entire cuff surface
for five minutes. Rinse continuously with distilled water for five minutes. Wipe off excess
water with sterile cloth and allow cuff to air dry.
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CAUTION: Do not iron cuff.
LOT 0 00000 000
Hauppauge, NY
ADC
!
CAUTION: Do not heat or steam sterilize cuff.
!
Manometer Quality Control
A Serial number and Lot number are automatically assigned to every aneroid during manufacturing, ensuring every item is "controlled".
The Serial Number can be located on the
faceplate of each aneroid (Figure 4).
The Lot number is located on the box end
label (Figure 5).
(Figure 5)
(Figure 4)
Serial Number
Lot Number
Standards
ANSI/AAMI/ISO 81060-1:2007 • EN/ISO 81060-1: 2012
Disposal
When your sphygmomanometer has reached its end of life, please be sure to dispose of
it in accordance with all regional and national environmental regulations. Devices that
have become contaminated should be disposed of in accordance with all local ordinances and regulations.
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Warranty
The manufacturer warrants its products against defects in materials and workmanship
under normal use and service as follows:
• Warranty service extends to the original retail purchaser only and commences
with the date of delivery.
Warranty duration is as follows:
Manometer Inflation System
5 YEARS 1 YEAR
10 YEARS 1 YEAR
20 YEARS 3 YEARS
LIFE 3 YEARS
*Refer to box end panel for specific warranty duration.
What is Covered: Calibration, repair, or replacement of parts and labor.
What is Not Covered: Transportation charges. Damages caused by abuse, misuse,
accident, or negligence. Incidental, special, or consequential damages. Some states
do not allow the exclusion or limitation of incidental, special, or consequential damages, so this limitation may not apply to you.
Implied Warranty: Any implied warranty shall be limited in duration to the terms of
this warranty and in no case beyond the original selling price (except where prohibited by law). This warranty gives you specific legal rights and you may have other
rights which vary from state to state.
To Obtain Warranty Service: Send item(s) postage paid to: Warranty Service Center, 55 Commerce Dr., Hauppauge, NY 11788. Please include your name and address, phone no., proof of purchase, and a brief note explaining the problem.
IB p/n 9360N-00 rev 7
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Printed in the U.S.A.
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