ADC CQ60698700 Diagnostix Pocket Aneroid Sphygmomanometer Instruction Manual
- June 6, 2024
- ADC
Table of Contents
- Device Description and Intended Use
- Symbol Definitions
- General Warnings ****
- Operation of Diagnostix Pocket Aneroids
- Operation of Diagnostix Palm Aneroids
- Connecting Palm Style Model: 804N
- Using the Trigger Valve
- Operation of Diagnostix Clock Aneroids
- Adcuff Intended Use
- Measurement Procedure
- Care and Maintenance
- Cuff Cleaning and Disinfecting
- Low-Level Disinfection
- Manometer Quality Control
- Standards
- Disposal
- Warranty
- Read User Manual Online (PDF format)
- Download This Manual (PDF format)
Diagnostix™ Aneroids
Pocket, Palm, Clock Type
Instructions for Use
ADC Aneroid Sphygmomanometer
(manometer, cuff, bladder, bulb and valve)
Thank you for choosing an ADC Diagnostix Aneroid Sphygmomanometer. Your new aneroid is designed to provide unrivaled durability and unparalleled comfort. Every component has been carefully designed to maximize performance. This Instructions for Use guide refers to ADC model series 700, 703, 705, 720, 728, 731, 732, 740, 750, 752, 778, and 788.
Device Description and Intended Use
ADC aneroid sphygmomanometers are used by professional healthcare providers and individuals trained in the auscultatory blood pressure technique to determine systolic and diastolic blood pressure in humans.
Contraindications: Aneroid sphygmomanometers are contraindicated for neonate use. Do not use with neonatal cuffs or neonate patients. Review the size chart for proper age and limb range usage (right).
Size Chart
Cuff | Size | Limb Range Inches | CM |
---|---|---|---|
Child | 7I | 3.5 to 5.5 | 9 to 14 |
Infant | 9C | 5.1 to 7.6 | 13 to 19.5 |
Sm. Adult | 10SA | 7.4 to 10.6 | 19 to 27 |
Adult | 11A | 9 to 15.7 | 23 to 40 |
Lg. Adult | 12X | 13.3 to 19.6 | 34 to 50 |
Thigh | 13T | 15.7 to 25.9 | 40 to 66 |
Bariatric | 12BX | 17.3 to 25.9 | 44 to 66 |
Symbol Definitions
The following symbols are associated with your ADC Diagnostix Aneroid
Symbol | Definition |
---|---|
Important warning/caution | |
Not made with natural rubber latex | |
Phthalate free | |
Circumference size | |
Meets the general safety and performance requirements of Regulation (EU) |
2017/745 of the European Union
| Authorized European representative’s information
| Manufacturer’s information
| Temperature limit
| Humidity
limitation
| Medical Device
****| Consult Instructions for Use
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
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 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.
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 to 104°F (10°C to 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 Diagnostix Pocket Aneroids
This booklet contains operating and maintenance information for the iagnostix
700, 720, 728, and 778 eries pocket aneroid sphygmomanometers. Please read and
retain.
Your Diagnostix brand pocket aneroid sphygmomanometer consists of an aneroid
manometer (gauge), complete inflation system (Adcuff calibrated nylon cuff,
latexfree inflation bladder, squeeze bulb, and Adflow valve), a zippered
carrying case, and operating instructions.
Most models are preassembled and ready for use. In units requiring assembly,
the bulb and valve should connect to the tube closest to the Index Line. The
gauge connects to the remaining tube.
Operation of Diagnostix Palm Aneroids
This booklet contains operating and maintenance information for the Diagnostix
703 and 788 Series, the Pediatric and General Practice multicuff kits, and the
731, 732, and System 5 portable multicuff kits. Please read and retain.
Your Diagnostix palm-style aneroid includes a manometer with integral bulb and
trigger air release valve (#804N), Adcuff calibrated cuff with Size Guide ™
marking system, bladder, bayonet-style connector (attached to bladder tubing),
zippered carrying case, and instruction booklet. ADC’s Multicuff Systems (731,
732, System 5, GPK, and PMK) contain the #804N manometer and a variety of
cuffs with single tube bladders, each equipped with a bayonet-style connector,
and a compartmentalized case.
Connecting Palm Style Model: 804N
Legacy Connector: Assemble the supplied luer slip connector into the connector port on top of palm gauge, rubber gasket side down. Make sure connector is fully seated in the connector port. Slide cuff tubing over the barbed end of the connector. Connector will friction fit onto the tubing of most commercially available ONE-tube cuff and bladder systems (Figure 1).
New 804N Connector: Insert metal bayonet connector into metal receiver
until it clicks (Figure 2).
To Release: Slide receiver collar downward toward gauge until connector
releases.
WARNING: Do NOT remove metal receiver from gauge.
WARNING: The palm style manometer is designed for use with ONE-tube
systems.
WARNING: To avoid damage to the instrument, do not force connector into
port.
Using the Trigger Valve
Deflation: Gently squeeze the bottom of the trigger to deflate the cuff.
Altering the pressure affects the deflation rate.
Rapid Exhaust: To exhaust remaining air after measurement is completed,
squeeze trigger until it clicks and locks in place.
**CAUTION:** Never force trigger.
Operation of Diagnostix Clock Aneroids
This booklet contains operating and maintenance information for the Diagnostix
750W series (wall mount), 752M series (mobile), and 750D series (desktop)
aneroid sphygmomanometers. Please read and retain.
Your Diagnostix 750/752 consists of a large “clockface” aneroid with easy-to-
read 6” dial, an integral swivel bracket/cuff storage compartment (wall series
only), complete inflation system (which includes the Adcuff nylon cuff with
Size Guide marking system, latex-free inflation bladder, bulb, and Adflow
valve), 8-foot length coiled tubing, luer connectors, mounting hardware, and
operating instructions. The Diagnostix 752M is mounted on a height adjustable,
Spider-Leg Important warning/caution representative’s information LATEX
Phthalate free Circumference size Manufacturer’s information Temperature limit
Humidity limitation Medical Device Consult Instructions for Use Not made with
natural rubber latex 158 ° F 85 Meets the general safety and performance
requirements of Regulation (EU) 2017/745 of the European Union 1434 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. ™ 5-leg mobile stand. The Diagnostix 750D is mounted on a desktop
stand.
To assemble the inflation system, connect coiled tubing to air inlet nipple at
bottom of gauge. Insert male luer adapter on bladder tubing into female
receptacle at free end of coiled tubing. Store folded inflation system in
swivel bracket behind gauge on 750W and 750D or in integral basket on 752M.
Adcuff Intended Use
ADC blood pressure cuffs are noninvasive and are intended for use with manual
and automated noninvasive blood pressure measurement devices.
ADC’s Size Guide marking system assures use of correct cuff size and proper
cuff alignment. Printed Index and Range markings and applicable limb range (in
cm) allow easy identification of the correct cuff size. An artery mark printed
on both sides indicates bladder midpoint for correct cuff positioning. A
convenient nylon gauge hang tab permits flexible use with either pocket
aneroids or mercury manometers. Hook-and-loop adhesive surface provides a
snug, infinitely variable fit and is designed to withstand a minimum of 30,000
open/close cycles.
Measurement Procedure
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. Prior to
measurement the patient should relax comfortably for five minutes and should
refrain from talking or moving during measurement. Observer should view
manometer in a direct line to avoid “parallax error.”
Apply the cuff
Adcuff nylon cuffs are specially designed to promote 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 the artery mark positioned directly over
the brachial artery. The bottom edge of the cuff should be positioned
approximately 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 3).
To verify a
correct fit, check that the Index Line falls between the two Range Lines
(Figure 4).
Inflate the cuff
Close the Adflow 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.
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 lowpitched Korotkoff (pulse) sounds.
Deflate the cuff
Open the valve to deflate the cuff gradually at a rate of 2-3 mmHg per second.
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 1
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
Pocket Gauge: After measurement, fully exhaust cuff then wrap cuff around
gauge and bulb and store in zippered carrying case.
Palm Gauge: After measurement, fully exhaust cuff and store in zippered
carrying case. If unit will not be used for an extended period of time, leave
the trigger valve in the full exhaust position.
Clock Gauge: After measurement, fully exhaust cuff then wrap cuff around
bulb and store in storage compartment.
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 safely be
stored at temperatures ranging from -4°F to 158°F (-20°C to 70°C) with a
relative humidity of 15% to 85%.
Manometer: Your Diagnostix brand pocket aneroid gauge (#800 or #802),
palm aneroid (#804N) or clock aneroid (#805) requires minimal care and
maintenance.
The manometer may be cleaned with a soft cloth but should not be dismantled
under any circumstances.
Should the indicator needle of the manometer rest outside the oval calibration
mark (Figure 5), 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.
NOTE: Store gauge with valve in full exhaust position. (Figure 5)
In the event that the gauge is ever in need of calibration, simply return to
ADC. Damaged or broken parts will be replaced as needed at a minimum charge.
Refer to the warranty for specific details of warranty coverage.
The manufacturer recommends a calibration check every 2 years.
Cuff Cleaning and Disinfecting
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.
CAUTION: Do not iron cuff.
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 6).
The lot number is located on the outside label of the manometer packaging
(Figure 7).
Standards
ANSI/AAMI/ISO 81060-1:2007, EN/ISO 81060-1:2012
Disposal
When your sphygmomanometer or any of its parts have reached their end of life, please be sure to dispose of them 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.
Warranty
ADC ® 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.
- Your Diagnostix™ manometer is warranted for life. The manometer is warranted to remain accurate to ±3mmHg (or the prevailing standard) over its full range when compared to a reference standard for life.
- Inflation system components (cuff, bladder, tubing, bulb, valves, and connectors) are warranted for three years.
What Is Covered: Replacement of parts, and labor.
What Is Not Covered: Transportation charges to ADC. 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.
To Obtain Warranty Service: Send item(s) postage paid to ADC, Attn:
Repair Dept., 55 Commerce Dr., Hauppauge, NY 11788. Please include your name
and address, phone no., proof of purchase, and a brief note explaining the
problem.
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 register your product visit us at
www.adctoday.com/support/warranty-
registration
FOR QUESTIONS, COMMENTS,
OR SUGGESTIONS CALL TOLL FREE:
1-800-ADC-2670
OR VISIT
www.adctoday.com/feedback
ADC ®
55 Commerce Drive
Hauppauge, NY 11788
U.S.A.
mdi Europa GmbH
Langenhagener Str. 71
30855 Langenhagen
GERMANY
Assembled, inspected, and packaged in the U.S.A.
tel: 631-273-9600
toll free: 1-800-232-2670
fax: 631-273-9659
www.adctoday.com
info@adctoday.com
IB p/n 9350N-00
rev 10 (6/3/2021)| Printed in the U.S.A.
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