ADC 790-12XN Wartungshandbuch

Aneroid Sphygmomanometer

Use, Care, & Maintenance

Device Description and Intended Use

An aneroid sphygmomanometer is used by professional healthcare providers and individu-

als trained in the auscultatory blood pressure technique to determine systolic and diastolic

blood pressure in humans.

Contraindications:

Aneroid sphygmomanometers are con-

traindicated for neonate use. Do not use with

neonatal cuffs or neonate patients. Review

the size chart (right) for proper age and limb

range usage.

General Warnings

A warning statement in this manual identifies a condition or practice which, if not cor-

rected 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 estab-

lished.

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 frequently

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 read-

ings.

WARNING: When using with an infant or child cuff, extra care must be taken to pre-

Cuff Size Limb Range

Inches CM

Infant 7 3.5 to 5.5 9 to 1

Child 9 5.1 to 7.6 13 to 19.5

Sm. Adult 10 7. to 10.6 19 to 27

Adult 11 9 to 15.7 23 to 0

Lg. Adult 12 13.3 to 19.6 3 to 50

Thigh 13 15.7 to 25.9 0 to 66

Size Chart

vent 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 de-

sired level.

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%- 5% (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-

tenance information for pocket aneroid

sphygmomanometers. Please read and re-

tain.

Your pocket aneroid sphygmo-

manometer consists of an aneroid

manometer (gauge), complete inflation

system, (latex-free inflation bladder,

squeeze bulb, and the valve), a zip-

pered carrying case, and operating in-

structions.

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.

Measurement Procedure

1. Patient P siti n

The patient should sit or lie comfortably. The arm should be fully supported on a flat sur-

face 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 manome-

ter in a direct line to avoid “Parallax error”.

2. Apply the cuff

Nylon cuffs are specially designed to promote the precisely accurate determination of blood

Cuff

Index Line

Hang

Tab

Gauge

Artery Mark

Bulb & Valve

Bladder &

Tubing

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 the ar-

tery mark positioned directly over the brachial ar-

tery. 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

Close the valve by turning thumbscrew clockwise.

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. P siti n the Steth sc pe

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.

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.

Left Arm

Tube

(Figure 1)

Select Smaller Cuff

▲

CORRECT

▲

Select Larger Cuff

▲

Care and Maintenance

STORAGE:

P cket 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 5%.

Man meter: 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 cir-

cumstances.

Gauge accuracy can be checked visually; simply be certain

the needle rests within the printed oval when the unit is fully

deflated (Figure 3).

Should the indicator needle of the manometer rest outside of

this calibration mark, then the manometer must be re-cali-

brated 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 spe-

cific 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 dis-

NOTE: Store gauge with

valve in full exhaust position.

(Figure 3)

Manometer Quality Control

A Serial number and Lot number are automatically as-

signed 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).

Standards

ANSI/AAMI/ISO 1060-1:2007 • EN/ISO 1060-1: 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.

Symbol Definitions

The following symbols are associated with your aneroid sphygmomanometer.

LOT 0 00000 000

Lot Number

(Figure 4)

Serial Number

(Figure 5)

infect, 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 contin-

uously with distilled water for five minutes. Wipe off excess water with sterile cloth and

allow cuff to air dry.

CAUTION: Do not iron cuff.

CAUTION: Do not heat or steam sterilize cuff.

Symb l Definiti n

Important Warning/Caution

Latex-Free

Circumference Size

Conforms to EU Standards

Symb l Definiti n

Authorized European

Represenative’s Information

Manufacturer’s Information

Temperature Limit

Humidity Limitation

°F

ADC

55 Commerce Drive

Hauppauge, NY 11788

U.S.A.

ADC (UK) Ltd.

Unit 6, PO1 1TH

United Kingdom

Inspected in the U.S.A.

Made in China

tel: 631-273-9600, 1-800-232-2670

fax: 631-273-9659

www.adctoday.com

email: info@adctoday.com

IB p/n 9360N-00 rev 5 english

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 durati n is as f ll ws:

Man meter Inflati n 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 C vered: Calibration, repair, or replacement of parts and labor.

What is N t C vered: 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 pro-

hibited by law). This warranty gives you specific legal rights and you may have other

rights which vary from state to state.

T Obtain Warranty Service: Send item(s) postage paid to: Warranty Service

Center, 55 Commerce Dr., Hauppauge, NY 117 . Please include your name and

address, phone no., proof of purchase, and a brief note explaining the problem.

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