ADC 720-11ABK User Manual

DiagnostixTMAneroids
®
Pocket, Palm, Clock Type
Use, Care, & Maintenance
1
ADC®Aneroid Sphygmomanometer
LATEX
°
F
(manometer, cuff, bladder, bulb and valve)
®
Thank you for choosing an ADC
DIAGNOSTIXTMAneroid Sphygmomanometer. Your new ADC®DIAGNOSTIXTManeroid is designed to provide unrivaled durability, and unparal­leled comfort. Every component has been carefully designed to maximize performance. This Use, Care, & Maintenance 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.
Size Chart
Contraindications:
Aneroid sphygmomanometers are con­traindicated for neonate use. Do not use with neonatal cuffs or neonate patients. Review the size chart (right) for proper age and limb range usage.
Cuff Size
Infant 7I 3.5 to 5.5 9 to 14
Child 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
Limb Range
Inches CM
Symbol Definitions
The following symbols are associated with your ADC® DiagnostixTMAneroid
Definition
ymbol
S
Authorized European
Represenat
Manufacturer’s I
Temperature Limit
Humidity Limitation
2
Definition
ymbol
S
Important Warning/Caution
N rubber
C
Conforms to EU Standards
ot
rcumf
i
made w
lat
erence Si
natural
ith
ex
ze
ve’s Information
i
nformation
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 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-
!
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 de­sired 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%-85% (non-condensing).
CAUTION: Extreme altitudes may affect blood pressure readings. Your device has
!
been designed for normal environmental conditions.
3
Operation of DiagnostixTMPocket Aneroids
This booklet contains operating and maintenance information for the DIAG-
TM
NOSTIX
700, 720, 728, and 778 Se-
Hang Tab
ries pocket aneroid sphygmomanometers. Please read and retain.
Your ADC DIAGNOSTIX aneroid sphygmomanometer consists of an aneroid manometer (gauge), com-
TM
brand pocket
Bulb & Valve
plete inflation system (ADCUFFTMcali­brated nylon cuff, latex-free inflation bladder, squeeze bulb, and the AD-
TM
FLOW
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.
Gauge
Artery Mark
Index Line
Bladder &
Tubing
Cuff
Operation of DiagnostixTMPalm
Connector Port
Trigger Valve
Cuff
Aneroids
This booklet contains operating and maintenance information for the DIAGNOSTIX
TM
703, 788 Series, System 3, Pediatric, General Practice, System 4 and System 5 Multicuff instruments. Please read and retain.
Your DIAGNOSTIX
palm style aneroid manometer with integral bulb and trigger air release valve (#804N), ADCUFF™ calibrated cuff with Size Guide™marking sys­tem, bladder, luer slip connector (attached to bladder tubing), zippered carrying case, and in­struction booklet. ADC®’s Multicuff Systems (System 3, 4, 5, GPK, and PMK) contain the #804N manometer and a variety of cuffs with single tube bladders, each equipped with a luer slip con­nector, and a compartmentalized case.
Gauge
Bladder Tubing
Artery Mark
4
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