Graham Field SONAR 14423 2 User Manual

14423-2 / 14423-4 / 14423-8  
ULTRASOUND POCKET DOPPLER  
USER MANUAL  
Important: Do not use the Pocket Doppler  
without first reading and understanding this  
manual! Save this manual for future use.  
Federal Law (USA) restricts this device to sale  
by or on the order of a physician. This product  
should not be used unless the operator has  
been instructed by a qualified healthcare pro-  
fessional.  
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1 INTRODUCTION  
This user manual contains important information and  
safety precautions for the Grafco Ultrasound Pocket Dop-  
pler. Before using the Pocket Doppler, please read and  
understand this entire user manual. Take special note of all  
safety precautions that begin “WARNING” and “CAUTION”.  
Save this user manual for future reference.  
Info: The most current version of this manual can be  
INTENDED USE OF THIS DEVICE  
The Grafco Ultrasound Pocket Doppler is intended for  
clinical use as an obstetrical evaluation tool. The Grafco  
Ultrasound Pocket Doppler may also be used for optional  
vascular monitoring. The Pocket Doppler is not intended  
to be used for treatment or diagnosis. Use the Pocket Dop-  
pler only as prescribed by a physician.  
WARNING: This device is not intended to be used  
for treatment or diagnosis. If Pocket Doppler results  
are ambiguous, please use other methods, such as a  
stethoscope, to verify immediately.  
WARNING: To ensure patient safety, use this device  
only with accessories recommended by GF Health  
Products, Inc., your GF authorized distributor, or your  
physician.  
INCLUDED FEATURES  
Mini USB Probe Socket  
Probe Detector  
Built-in Speaker  
Adjustable Volume  
Alkaline Battery (9V)  
Low Battery Detector / Indicator  
Obstetrical or Vascular Monitoring  
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OPTIONAL ACCESSORIES  
The following accessories for use with the Grafco Ultrason-  
ic Pocket Doppler are available from your GF Health Prod-  
Item No. Product Description  
4001GF  
Coupling Gel, case of 12 0.25 liter bottles  
4002GF  
Coupling Gel, 5 liter bottle  
14423-2P 2.0 MHz Water-Resistant Probe  
14423-4P 4.0 MHz Water-Resistant Vascular Probe  
14423-8P 8.0 MHz Water-Resistant Vascular Probe  
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2 SAFETY INFORMATION  
Safety Guidance  
This unit has internally  
powered equipment,  
and the degree of shock  
protection is type B  
Type B protection means that this  
product is in accordance with  
permitted leakage currents and  
dielectric strengths of IEC 60601-1.  
SAFETY PRECAUTIONS  
The safety statements presented in this chapter refer  
to the basic safety information that the operator of the  
Pocket Doppler shall pay attention to and abide by. There  
are additional safety statements in other chapters or sec-  
tions, which may be the same as or similar to the follow-  
ing, or specific to the operations. WARNING and CAUTION  
statements must be observed. To avoid the possibility of  
injury, observe the following precautions during the opera-  
tion of the instrument.  
Please note the following special statements, used through-  
out this manual, and their significance:  
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 moderate  
or minor personal injury.  
s NOTICE: Indicates a potential hazard or unsafe prac-  
tice 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.  
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WARNINGS  
WARNING: Federal Law (USA) restricts this device to  
sale by or on the order of a physician. This product  
should not be used unless the operator has been in-  
structed by a qualified healthcare professional.  
WARNING: Do not use the Grafco Pocket Doppler in a  
flammable atmosphere where concentrations of flam-  
mable anesthetics or other materials may occur.  
WARNING: Do not expose batteries to heat.  
WARNING: Do not attempt to charge alkaline batter-  
ies; they may leak or catch on fire.  
WARNING: DO NOT simultaneously touch signal in-  
put or output connector and the patient.  
WARNING: Accessory equipment connected to the  
analog and digital interfaces must be certified accord-  
ing to the respective IEC standards (e.g. IEC 950 for  
data processing equipment and IEC 60601-1 for medi-  
cal equipment). Furthermore all configurations shall  
comply with the valid version of the system stan-  
dard IEC 60601-1-1. Anyone who connects additional  
equipment to the signal input connector or signal  
output connector configures a medical system, and is  
therefore responsible that the system complies with  
the requirements of the valid version of the system  
standard IEC 60601-1-1. If in doubt, consult your GF  
Health Products, Inc. authorized distributor.  
WARNING: The Grafco Pocket Doppler is a tool to aid  
the healthcare professional and should not be used in  
place of normal fetal monitoring.  
WARNING: Exposure to ultrasound should be kept as  
low as reasonably achievable. This is considered to  
be good practice and should be observed at all times.  
WARNING: Replace the battery at least 6 feet (1.5 me-  
ters) from the patient.  
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WARNING: Do not the use Pocket Doppler if the bat-  
tery cover is open.  
WARNING: Use only those probes provided by GF  
Health Products, Inc. intended to be used with the  
Grafco Pocket Doppler.  
WARNING: Do not stretch the probe cable further  
than 6.5 feet (2 meters).  
WARNING: Electromagnetic Interference: Before op-  
eration, ensure that the environment in which the de-  
vice is operated is not subject to any source of strong  
electromagnetic interference, such as radio transmit-  
ters, mobile telephones, etc.  
WARNING: The following safety checks/tests must be  
performed at least once every two years or as speci-  
fied in your facility's test and inspection protocol, by  
a qualified person with adequate training, knowledge,  
and practical experience:  
• Inspect the equipment for mechanical and func-  
tional damage.  
• Ensure the safety labels are legible.  
• Verify that the device functions properly as de-  
scribed in this manual.  
• Test according to the pregnant woman's leakage  
current (IEC 60601-1/1988: Limit: 100 uA (B)).  
The leakage current should never exceed the speci-  
fied limit. Record the data and store with the Grafco  
Pocket Doppler. If the device is not functioning prop-  
erly or fails any of the above tests, contact GF Health  
Products, Inc. Technical Support at the phone number  
on the back cover, or your GF authorized distributor.  
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NOTICES  
s NOTICE: The main unit of the Grafco Pocket Doppler  
is designed for continuous normal operation. Do not  
immerse or submerge in any liquid.  
s NOTICE: Keep the Pocket Doppler and its environ-  
ment clean and dust-free. Protect the device from vi-  
bration, corrosive medicine, and high temperatures.  
s NOTICE: Do not use high-temperature sterilizing pro-  
cess, low temperature steam, E-beam, or gamma ra-  
diation sterilization on this device or its accessories.  
s NOTICE: If the Pocket Doppler will not be used for a  
prolonged period of time, remove the battery from the  
device.  
s NOTICE: Keep the battery away from objects or mate-  
rials with static electric charges.  
s NOTICE: If the battery terminals become dirty, wipe  
them with a clean, dry cloth before using the battery.  
s NOTICE: Batteries have life cycles. If the battery use  
time shortens noticeably, the battery's life cycle is  
over. Replace the old battery with a new one of the  
same size and type. Use only batteries recommended  
by GF Health Products, Inc.  
s NOTICE: Remove a battery whose life cycle is over  
from the monitor immediately.  
s NOTICE: For information on installing and removing  
the battery from the monitor, see Section 5, SETUP.  
s NOTICE: Dispose of the battery in accordance with lo-  
cal regulations.  
s NOTICE: Do not dispose of this device with house-  
hold waste. Dispose of this device in accordance with  
your local laws and regulations.  
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SYMBOLS  
Attention: Refer to accompanying documents (this manual).  
This item is compliant with Medical Device Directive 93/42/  
EEC of June 14, 1993, a directive of the European Economic  
Community.  
This symbol consisting of two parts, see below.  
Indicates that the equipment should be disposed of according  
to local regulation for separate collection after its useful life.  
Do not dispose of this device with household waste.  
Indicates that the equipment is put on the market after 13  
August 2005.  
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3 HANDLING  
GF HEALTH PRODUCTS, INC. FREIGHT POLICY  
For your protection, read carefully  
The carrier accepted this merchandise “in good condition”  
and is responsible for safe delivery. Before signing the  
freight bill, inspect the shipment carefully for damage or  
missing pieces.  
Apparent loss or damage  
Should visual inspection show loss or damage, this MUST  
be noted on the freight bill and signed by the carrier's  
agent. Failure to do so may result in the carrier failing to  
honor the claim. Please contact the carrier to obtain the  
paperwork necessary to file a claim or contact GF Health  
Products, Inc. Customer Service at the number on the back  
cover of this manual.  
Concealed loss or damage  
If damage is discovered after delivery is made, a concealed  
damage claim must be entered with the freight carrier.  
When this occurs, make a written request to the carrier for  
inspection. This request for inspection must be made with-  
in 15 days of delivery. The carrier will provide all paper-  
work necessary to file a concealed damage or loss claim,  
since such damage or loss is the carrier's responsibility.  
UNPACKING  
Info: Unless the Pocket Doppler is to be used immediately,  
retain containers and packing materials for storage until  
Pocket Doppler use is required.  
1. Check for obvious damage to the carton or its contents.  
If damage is evident, please notify the carrier and your  
GF Health Products, Inc. authorized distributor.  
2. Remove all loose packing from the carton.  
3. Carefully remove all the components from the carton.  
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Inspection  
Check the Pocket Doppler for nicks, dents, scratches, me-  
chanical or other damage. Check all the cables and acces-  
sories.  
STORAGE  
Store the repackaged Pocket Doppler in a dry area.  
s NOTICE: Ensure that the temperature at the Pocket  
Doppler's location during storage does not fall below  
~14°F (-10°C) or exceed ~131°F (55°C).  
s NOTICE: Ensure that relative humidity at the Pocket  
Doppler's location during storage does not exceed  
93%.  
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4 ULTRASOUND POCKET DOPPLER  
AND ACCESSORIES  
APPEARANCE AND FEATURES  
The following figures illustrate the Pocket Doppler with the  
2.0 MHz water-resistant probe, and accompanying tables  
describe labeled features.  
Front Panel  
Feature Function  
Display  
Displays system info  
Panel  
System status The system status LED is at the left bottom  
corner of the display panel. Please see  
the following table for significance of LED  
indicators.  
LED  
LED  
LED  
Significance  
Illumination Illumination  
Color  
Green  
Condition  
Constant  
Flashing  
Power on  
Probe disconnected or not  
properly connected  
Orange  
Flashing  
Battery too low for  
operation; replace battery  
immediately  
Brand  
Brand of Pocket Doppler  
Probe  
Speaker  
The Probe is used to perform ultrasound monitoring  
The built-in speaker makes the fetal sounds audible  
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Power  
Button  
Turns the Ultrasound Pocket Doppler ON or  
OFF  
Probe  
The probe connects here to the Ultrasound Pocket Doppler  
Socket  
Jack  
Definition  
Power Supply  
Signal  
1
2
3
4
5
6
Probe Coding 1  
Probe Coding 2  
Probe Coding 3  
(Shell) GND  
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Rear Panel  
Feature  
Function  
Pocket Clip  
Attaches Pocket Doppler to pocket  
Attachment  
Battery  
Opens to install/replace battery  
Attaches probe to Pocket Doppler  
Compartment  
Probe Frame  
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Top Panel  
Feature Function  
Socket  
Name  
Picture  
Function  
Charge  
Socket  
Not used  
Earphone  
Socket  
Connect earphone  
Signal  
1
2
3
4
5
GND  
Interface  
Signal  
Signal  
Signal  
Signal  
Warning  
Refer to accompanying documents  
(this user manual)  
WARNING: Accessory equipment connected to the  
analog and digital interfaces must be certified accord-  
ing to the respective IEC standards (e.g. IEC 950 for  
data processing equipment and IEC 60601-1 for medi-  
cal equipment). Furthermore all configurations shall  
comply with the valid version of the system stan-  
dard IEC 60601-1-1. Anyone who connects additional  
equipment to the signal input connector or signal  
output connector configures a medical system, and is  
therefore responsible that the system complies with  
the requirements of the valid version of the system  
standard IEC 60601-1-1. If in doubt, consult your GF  
Health Products, Inc. authorized distributor.  
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Left Panel  
Feature  
Function  
Volume Control  
Adjust  
volume  
Increase volume:  
Rotate volume knob  
clockwise  
Decrease volume:  
Rotate volume knob  
counter-clockwise  
MODE Button  
Not used  
START/STOP Button  
REC/PLAY Button  
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POCKET DOPPLER WATER-RESISTANT PROBES  
The 2.0 MHz, 4.0 MHz, and 8.0 MHz water-resistant probes  
connect to the main unit of the Grafco Pocket Doppler via  
the probe socket. The following table lists and describes  
the main information on each probe's label in order of ap-  
pearance:  
Pocket Doppler Water-Resistant Probe Label Table  
Picture of Probe  
Probe Label  
Text  
2.0 MHz  
4.0 MHz  
8.0 MHz  
Water-Resistant Water-Resistant Water-Resistant  
Probe  
Vascular  
Probe *  
Vascular  
Probe *  
CD  
Continuous Wave Doppler  
X.0 (Central  
Central  
frequency =  
2.0 MHz  
Central  
frequency =  
4.0 MHz  
Central  
frequency =  
8.0 MHz  
Frequency)  
A
Probe version number  
Probe Serial Number  
SNxxxxx:  
Water-Resistant  
IPX8  
The probe is water-resistant  
Water Ingress Protection Code, which indicates  
this probe can work continuously for 5 hours when  
immersed in water up to one meter deep.  
(Water-Resistant)  
* Vascular probes are used to monitor arteries and veins  
BATTERY  
See Section 5, SETUP, for battery installation and replace-  
ment instructions.  
WARNING: Use only 9V alkaline batteries (IEC Type  
No. 6LR61/6LF22 or equivalent) in this device.  
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5 SETUP  
INSTALLING OR REPLACING THE BATTERY  
WARNING: Ensure that Pocket Doppler power is off  
before replacing the battery.  
WARNING: Install/replace the battery at least 6 feet  
(1.5 meters) from the patient.  
WARNING: Use only 9V alkaline batteries (IEC Type  
No. 6LR61/6LF22 or equivalent) in this device.  
battery socket  
battery compartment  
battery connector  
battery cover  
battery installation  
1. Open the battery compartment: Slide the battery cover  
in the direction of the arrow on the battery cover (see  
above picture).  
2. If replacing the battery, remove the old battery.  
3. A battery connector is located in the battery compart-  
ment. Attach a new 9V battery to the connector.  
4. Install the connected battery in the battery compart-  
ment.  
5. Slide the battery cover back to close the compartment.  
s NOTICE: If the Pocket Doppler will not be used for a  
prolonged period of time, remove the battery from the  
device.  
s NOTICE: Keep the battery away from objects or mate-  
rials with static electric charges.  
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s NOTICE: If the battery terminals become dirty, wipe  
them with a clean, dry cloth before using the Pocket  
Doppler.  
s NOTICE: Batteries have life cycles. If the battery use  
time shortens noticeably, the battery's life cycle is  
over. Replace the old battery with a new one of the  
same size and type. Use only batteries recommended  
by GF Health Products, Inc.  
s NOTICE: Remove a battery whose life cycle is over  
from the Pocket Doppler immediately.  
s NOTICE: Dispose of the old battery in accordance  
with local regulations.  
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6 OPERATION  
PROBE OPERATION  
Removing the Probe from the Pocket Doppler  
s NOTICE: Do not drag or drop the probe. Do not dis-  
connect the probe from the Pocket Doppler.  
1. The probe is installed in Pocket Doppler probe frame  
(left picture above). Hold the Pocket Doppler main unit  
with one hand and hold the top of the probe with the  
other hand.  
2. Gently remove the top of the probe from the Pocket  
Doppler probe frame (center picture above).  
3. Remove the entire probe from Pocket Doppler probe  
frame (right picture above).  
Placing the Probe in the Pocket Doppler  
s NOTICE: Do not drag or drop the probe. Do not dis-  
connect the probe from the Pocket Doppler.  
1. Hold the Pocket Doppler main unit with one hand and  
hold the probe with the other hand.  
2. Gently guide the middle of the probe into the Pocket  
Doppler's probe frame (center picture above).  
3. Gently replace the top of probe entirely into the Pocket  
Doppler's probe frame (left picture above).  
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Swapping Probes  
s NOTICE: Do not drag or drop the probe or the probe  
connector.  
The Pocket Doppler is shipped with one probe connected.  
To replace the connected probe with another Pocket Dop-  
pler probe:  
1. Follow steps 1-3 in previous section, Removing the  
Probe from the Pocket Doppler.  
2. Remove the connector: Grasp  
probe connector body and gen-  
tly pull out from Pocket Doppler  
probe socket.  
3. Connect the new probe's con-  
nector: Grasp probe connec-  
tor body and gently insert into  
Pocket Doppler's probe socket.  
Pocket Doppler is shown at  
right with disconnected probe.  
s NOTICE: Place the unused probe in a secure location.  
When the Pocket Doppler is not used for a long time,  
store Doppler and probe in original packaging (see  
Maintenance/Storage section for proper storage con-  
ditions).  
TURNING ON THE POCKET DOPPLER  
Press the front panel POWER button to turn on the Pocket  
Doppler.  
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FETAL HEART (FH) MONITORING  
FH Monitoring with 2.0 MHz Water-Resistant Probe  
Refer to picture at right. The au-  
dio fetal heart beat is sent out via  
the built-in speaker or attached  
earphone.  
1. Palpate for the fetus position  
to find the best location to  
place the probe and hear the  
fetal heart rate.  
2. Apply a liberal amount of gel to the probe head.  
3. Place the probe head on the desired location. Assure  
that good coupling of the gel to the skin is achieved; the  
Fetal Heart rate will not be heard if adequate gel is not  
used and air is between the probe head and skin.  
4. Slowly move the probe until a clear heart rate is heard.  
5. Adjust the volume to the desired level.  
WARNING: It is not possible to monitor FHR unless  
an audible fetal heart signal is present. The fetal  
pulse can be distinguished from the maternal pulse  
by feeling the mother’s pulse during the examination.  
WARNING: For best quality audio, place the probe in  
the optimum position.  
WARNING: For best quality audio, avoid positions  
with strong placental sounds (swishing) or fetal cord  
pulse (indistinct pulse at fetal rate).  
WARNING: If the fetus is in the cephalic position and  
the mother is supine, the clearest heart sound will  
normally be found on the midline below the umbili-  
cus. During monitoring, prolonged lying in the supine  
position should be avoided. Sitting up or lateral posi-  
tions are preferable and may be more comfortable for  
the mother.  
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VASCULAR MONITORING WITH 4.0 OR 8.0 MHZ  
PROBE (OPTIONAL)  
The 4.0 MHz and 8.0 MHz probes can be used to perform  
vascular monitoring assessment of blood flow.  
The 8.0 MHz probe is used for more superficial evaluation  
than the 4.0 MHz probe. Refer to the following probe site  
illustration to determine the best probe to utilize.  
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1. Apply a liberal amount of gel on the site to be exam-  
ined.  
2. Place the probe so that the head is at least at 45º to the  
vessel to be examined.  
3. Adjust the position of the probe to obtain the loudest  
audio signal. For best results, keep the probe as still as  
possible once the optimum position is located.  
4. Adjust the audio volume as necessary.  
Info: Arteries emit high-pitched rhythmical pulsation  
sounds, while veins emit non- rhythmical pulsation sounds  
similar to rushing wind.  
TURNING OFF THE POCKET DOPPLER  
1. When the session is finished, press the front panel  
POWER button to turn off the Pocket Doppler.  
2. Use a clean, dry, non-abrasive cloth to gently wipe off  
the remaining gel from the probe. After thoroughly  
cleaning the probe, replace it in the Pocket Doppler  
probe frame.  
REPLACING THE BATTERY  
When the Pocket Doppler battery power is low, turn the  
power off and replace the battery. See Section 5, SETUP,  
for instructions on battery replacement.  
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7 MAINTENANCE  
WARNING: Failure on the part of the responsible facil-  
ity employing the use of this equipment to implement  
a satisfactory maintenance schedule may cause un-  
due equipment failure and possible health hazard.  
MAINTENANCE  
WARNING: Before use, inspect the Pocket Doppler  
and probe(s) to ensure there is no visible evidence  
of damage which may affect the functioning of the  
device or pregnant woman’s safety, or create the po-  
tential for the device to operate in an unsafe manner.  
Thereafter, inspect the device for evidence of damage  
at least once each week. If damage is evident or sus-  
pected, contact GF Health Products, Inc. Technical  
Service at the number on the back cover or your GF  
authorized distributor before use.  
WARNING: The following safety checks/tests must be  
performed at least once every two years or as speci-  
fied in your facility's test and inspection protocol, by  
a qualified person with adequate training, knowledge,  
and practical experience:  
• Inspect the equipment for mechanical and func-  
tional damage.  
• Ensure the safety labels are legible.  
• Verify that the device functions properly as de-  
scribed in this manual.  
• Test according to the pregnant woman's leakage  
current (IEC 60601-1/1988: Limit: 100 uA (B)).  
The leakage current should never exceed the speci-  
fied limit. Record the data and store with the Grafco  
Pocket Doppler. If the device is not functioning prop-  
erly or fails any of the above tests, contact GF Health  
Products, Inc. Technical Support at the phone number  
on the back cover, or your GF authorized distributor.  
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s NOTICE: Keep the Pocket Doppler and its environ-  
ment clean and dust-free. Protect the device from vi-  
bration, corrosive medicine, and high temperatures.  
s NOTICE: Do not use high-temperature sterilizing pro-  
cess, low temperature steam, E-beam, and/or gamma  
radiation sterilization on this device or its accesso-  
ries.  
CLEANING  
WARNING: Before cleaning the Pocket Doppler or  
probes, turn the Pocket Doppler power off and re-  
move the battery.  
s NOTICE: Do not use strong solvent such as acetone  
to clean Pocket Doppler or probe.  
s NOTICE: Do not use an abrasive such as steel wool  
or metal polish to clean Pocket Doppler or probe.  
s NOTICE: Do not allow any liquid to enter the probe  
socket while cleaning the Pocket Doppler or probe.  
Cleaning the Pocket Doppler  
s NOTICE: Do not immerse Pocket Doppler. Do not al-  
low liquid to enter the ultrasound system.  
s NOTICE: Do not pour liquids on the Pocket Doppler  
while cleaning.  
1. Keep the exterior surface of the Pocket Doppler clean  
and free of dust and dirt.  
2. Clean the exterior surface of the unit with a clean, dry,  
nonabrasive cloth.  
3. If necessary, clean the unit with a clean cloth dampened  
with soap and water, then immediately wipe dry with a  
clean, dry, non-abrasive cloth.  
s NOTICE: Do not allow any liquid or cleaning solution  
to remain on the surface of the Pocket Doppler or  
probe after cleaning.  
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Cleaning the Pocket Doppler Probe  
s NOTICE: Do not allow liquid to enter the ultrasound  
system.  
s NOTICE: Do not pour liquids on the probe while  
cleaning.  
The Pocket Doppler probe’s acoustic surface is fragile and  
must be handled with care.  
1. To prolong the life of the probe, after each use, gently  
wipe off the remaining gel from the probe with a clean,  
dry, non-abrasive cloth.  
2. After thoroughly cleaning the probe, replace it in the  
Pocket Doppler probe frame.  
3. If necessary, wipe the external surface of probe with  
70% ethanol or isopropranol alcohol.  
4. Allow to air dry.  
s NOTICE: Do not allow any liquid or cleaning solution  
to remain on the surface of the probe after cleaning.  
14423-INS-LAB-RevD11  
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DISINFECTION  
Disinfecting the Pocket Doppler Probe  
s NOTICE: Do not allow any liquid to enter the probe  
socket while disinfecting or immersing the probe.  
1. Clean the exterior surface of the probe as recommend-  
ed in the previous section.  
2. To disinfect the probe, immerse the probe in a solution  
of Benzalkonium Bromide, 0.5% Chlorhexidine, 2% Glu-  
taraldehyde, or 75% ethanol.  
3. Wipe the probe with a clean, dry, non-abrasive cloth to  
remove any remaining moisture.  
s NOTICE: Do not allow any liquid or cleaning solution  
to remain on the surface of the probe after cleaning.  
14423-INS-LAB-RevD11  
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8 SPECIFICATIONS  
Model Number  
14423-2  
Ultrasonic Pocket Doppler  
with 2.0 MHz probe  
and Name  
14423-4  
Ultrasonic Pocket Doppler  
with 4.0 MHz probe  
14423-8  
Ultrasonic Pocket Doppler  
with 8.0 MHz probe  
Safety  
Complies with: EN 60601-1/1990  
Classification  
Anti-electric  
Shock Type  
Internally powered equipment  
Anti-electric  
Shock Degree  
Type B equipment  
Degree of  
Protection  
against  
Harmful  
Ingress of  
Water  
Main Unit  
Non-protected  
2.0 MHz  
Water-Resistant  
Probe  
IPX8 Water  
Ingress  
Protection  
Code, which  
indicates  
4.0 MHz  
Water-Resistant  
Vascular Probe  
this probe  
can work  
continuously  
for 5 hours  
when being  
immersed in  
water less than  
1 meter deep  
8.0 MHz  
Water-Resistant  
Vascular Probe  
Degree of  
Safety in  
Presence of  
Flammable  
Gases  
Equipment not suitable for use in  
presence of flammable gases  
Working  
System  
Continuous running equipment  
Group I Class B  
EMC  
14423-INS-LAB-RevD11  
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Physical  
Size (Width x  
3.35 x 1.26 x 5.43 inches  
Characteristics  
Depth x Height) (85 x 32 x 138 mm)  
Weight  
.64 lb (290 ±5g)  
(including a  
battery and a  
probe)  
Environment  
Working  
Temperature  
Humidity  
41°F ~ 104°F  
(5°C ~ 40°C)  
≤80% RH  
Atmospheric  
Pressure  
12.47 ~ 15.37 psi  
(86 ~ 106 kPa)  
Transport and Temperature  
Storage  
14°F ~ 131°F (-  
10°C ~ +55°C)  
Humidity  
≤93% RH  
Atmospheric  
Pressure  
12.47 ~ 15.37 psi  
(86 ~ 106 kPa)  
FHR  
FHR Measuring 50 bpm ~ 210 bpm  
Range  
Performance  
Resolution  
Accuracy  
0.5W  
1 bpm  
±3 bpm  
Audio Output  
Power  
Battery  
Battery Type  
9 volt DC alkaline battery, IEC Type  
Recommended No. 6LR61/6LF22 or equivalent  
Battery Stand- > 10 hours  
by Time  
14423-INS-LAB-RevD11  
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Ultrasound  
Nominal  
Frequency  
2.0 MHz  
Water-Resistant  
Probe  
2.0 MHz  
4.0 MHz  
Water-Resistant  
Vascular Probe  
4.0 MHz  
8.0 MHz  
Water-Resistant  
Vascular Probe  
8.0 MHz  
Working  
Frequency  
2.0 MHz  
2.0 MHz ±10%  
4.0 MHz ±10%  
8.0 MHz ±10%  
Water-Resistant  
Probe  
4.0 MHz  
Water-Resistant  
Vascular Probe  
8.0 MHz  
Water-Resistant  
Vascular Probe  
P-  
< 1MPa  
Iob  
< 10 mW/cm2  
< 100mW/cm2  
Ispta  
Working Mode Continuous Wave Doppler  
Effective  
2.0 MHz  
245mm2 ±15%  
32mm2 ±15%  
14mm2 ±15%  
Radiating Area Water-Resistant  
of Transducer Probe  
4.0 MHz  
Water-Resistant  
Vascular Probe  
8.0 MHz  
Water-Resistant  
Vascular Probe  
14423-INS-LAB-RevD11  
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9 LIMITED WARRANTY  
GF Health Products Inc. warrants this product to be free from  
manufacturing defects in material and workmanship for  
its period of warranty that is in accordance with industry  
standards. This warranty is extended only to the original  
purchaser/consumer or dealer/non-consumer of this new  
product and to no other purchaser or transferee.  
GF Health Products, Inc. warrants the Grafco Pocket Doppler  
and its components to be free from defects in workmanship  
and materials for a period of one year.  
The Warranty period for the consumer commences on the  
first date a product is delivered to consumer by seller/dealer.  
If the product is rented or leased, the warranty period com-  
mences on the invoice date from GF Health Products, Inc.  
A copy of the invoice showing date of purchase must be  
provided when submitting warranty claims. When proof  
of purchase date is not provided, warranty coverage shall  
commence upon GF Health Products, Inc.’s invoice date to  
the dealer/purchaser.  
If within the warranty period, the product or component part  
is proven to GF Health Products, Inc.’s satisfaction to be defec-  
tive, GF Health Products, Inc. shall provide, at its option, one  
of the following: (1) repair or replacement of any defective or  
nonconforming part or product or (2) a credit and/or refund  
of the original selling price. GF HEALTH PRODUCTS, INC.’S  
SOLE OBLIGATION AND YOUR EXCLUSIVE REMEDY UNDER  
THIS WARRANTY SHALL BE LIMITED TO SUCH REPAIR, RE-  
PLACEMENT, CREDIT AND/OR REFUND. This warranty does  
not include any labor charges incurred in replacement part(s)  
installation or any associated freight or shipping charges to  
the manufacturer.  
For warranty service, please contact the authorized dealer  
from whom you acquired your GF Health Products, Inc. prod-  
uct. Upon receiving notice of an alleged defect in a product,  
GF Health Products, Inc. will issue a return authorization. The  
defective product or part(s) must then be returned, at the  
14423-INS-LAB-RevD11  
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purchaser’s cost, for warranty inspection using the serial  
number as identification (or, if the product is not serialized,  
lot number and date code) within thirty (30) days of return  
authorization issue date. In the event you do not receive sat-  
isfactory warranty service, please contact GF Health Products,  
Inc. at the address below. DO NOT return products to our  
factory without prior authorization.  
LIMITATIONS AND EXCLUSIONS: The foregoing warranty shall  
not apply to serial numbered products if the serial number  
has been removed or defaced. Products subjected to negli-  
gence, abuse, misuse, improper operation, improper main-  
tenance, improper cleaning, improper storage, or damages  
beyond GF Health Products, Inc.’s control are not covered by  
this warranty, and that evaluation shall be solely determined  
by GF Health Products, Inc. This warranty shall not apply to  
problems arising from normal wear and tear or failure to  
follow instructions. The warranty shall also not apply to  
products modified without GF Health Products, Inc.’s express  
written consent; nor shall it apply if parts not manufactured  
by GF Health Products, Inc., or if parts not complying with  
original equipment specifications are added to GF Health  
Products, Inc. products, or if the product or part is serviced  
by an entity not authorized by GF Health Products, Inc.  
THE FOREGOING WARRANTY IS EXCLUSIVE AND IN  
LIEU OF ALL OTHER EXPRESS WARRANTIES AND  
IMPLIED WARRANTIES, INCLUDING BUT NOT LIM-  
ITED TO THE IMPLIED WARRANTIES OF MERCHANT-  
ABILITY AND FITNESS FOR A PARTICULAR PURPOSE,  
AND SHALL NOT EXTEND BEYOND THE DURATION  
OF THE EXPRESS WARRANTY PROVIDED HEREIN,  
AND THE REMEDY FOR VIOLATIONS OF ANY IMPLIED  
WARRANTY SHALL BE LIMITED TO THE REPAIR, RE-  
PLACEMENT, CREDIT AND/OR REFUND OF THE DEFEC-  
TIVE PRODUCT OR PART PURSUANT TO THE TERMS  
CONTAINED HEREIN. GF HEALTH PRODUCTS, INC.  
SHALL NOT BE LIABLE FOR ANY CONSEQUENTIAL  
OR INCIDENTAL DAMAGES WHATSOEVER.  
14423-INS-LAB-RevD11  
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This warranty gives you specific legal rights and you may also  
have other legal rights which vary from state to state (prov-  
ince to province). Some states (provinces) do not allow the  
exclusion or limitation of incidental or consequential damage,  
or limitation on how long an implied warranty lasts, so the  
above exclusion and limitations may not apply to you.  
The warranties contained herein contain all the representa-  
tions 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.  
GF Health Products, Inc. (“Graham-Field”)  
2935 Northeast Parkway  
Atlanta, GA 30360  
Tel 770-368-4700  
14423-INS-LAB-RevD11  
34  
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10 APPENDIX A, EC DECLARATION OF  
CONFORMITY  
EC Declaration of Conformity  
Manufactured for  
GF Health Products, Inc., 2935 Northeast Parkway,  
Atlanta, GA 30360  
Product  
Ultrasound Pocket Doppler  
(MDD, Annex IX): IIa  
Classification  
We herewith declare that the above mentioned product(s) meet the  
transposition into national law, the provisions of Council Directive  
93/42/EEC of 14 June 1993 concerning medical devices - as amended by  
Directive 98/79/EC on in vitro diagnostic medical devices.  
All supporting documentation is retained at the premises of the  
manufacturer.  
Directives  
General Applicable Directives: Medical Device  
Directive: COUNCIL DIRECTIVE 93/42/EEC of 14  
June 1993 concerning medical devices (MDD 93/42/  
EEC).  
Standards applied EN ISO 9001, ISO13485, EN ISO14971, EN ISO10993-  
1, IEC 601-1, EN 60601-1-1, BS EN 60601-1-4, IEC  
60601-1-2, EN 61157, EN 1041, EN 60417-2-2000,  
IEC/TR 60878-2003, EN 980, EN 55011, ISO 1000, YY  
0111-93, EN 61266, EN ISO 780 , GB/T 14740, GB/T  
15464  
Notified Body  
TÜV SÜD Product Service GmbH, Ridlerstr 65, D-  
80339 MÜnchen, Germany.  
Identification  
number  
14423-INS-LAB-RevD11  
35  
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11 APPENDIX B, EMC INFORMATION  
GUIDANCE AND MANUFACTURER’S  
DECLARATION  
Electromagnetic Emissions—for all Equipment  
and Systems  
Guidance and manufacturer’s declaration—  
electromagnetic emission  
The Grafco Ultrasound Pocket Doppler is intended for use in the  
electromagnetic environment specified below. Do not use the system in  
environments which do not comply with the specifications listed below.  
Emission  
Compliance  
Electromagnetic environment–  
test  
guidance  
RF emission Group 1  
CISPR 11  
The Grafco Ultrasound Pocket Doppler  
uses RF energy only for its internal function.  
Therefore, its RF emissions are very low  
and are not likely to cause any interference  
in nearby electronic equipment.  
RF emission Class B  
CISPR 11  
The Grafco Ultrasound Pocket Doppler  
is suitable for use in all establishments,  
including domestic establishments and  
those directly connected to the public  
low-voltage power supply network that  
supplies buildings used for domestic  
purposes.  
Electromagnetic Immunity—for all Equipment  
and Systems  
Guidance and manufacture’s declaration—electromagnetic  
immunity  
The Grafco Ultrasound Pocket Doppler is intended for use in the  
electromagnetic environment specified below. Do not use the system in  
environments which do not comply with the specifications listed below.  
Immunity IEC 60601 Compliance Electromagnetic  
test  
test level level  
environment—guidance  
Electrostatic ±6 kV  
±6 kV  
Floors should be wood,  
discharge contact ±8 contact ±8  
concrete or ceramic tile. If  
floor is covered with synthetic  
material, the relative humidity  
should be at least 30% RH.  
(ESD) IEC kV air  
61000-4-2  
kV air  
14423-INS-LAB-RevD11  
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Electromagnetic Immunity—for all Equipment  
and Systems that are not Life-Supporting  
Guidance and manufacturer’s declaration—  
electromagnetic immunity  
The Grafco Ultrasound Pocket Doppler System is intended for use in the  
electromagnetic environment specified below. Do not use the system in  
environments which do not comply with the specifications listed below.  
Immunity IEC 60601 Compliance Electromagnetic  
test  
test level level  
environment—guidance  
Radiated  
RF IEC  
3 V/m 80  
3 V/m  
Portable and mobile RF  
MHz to 2.5  
communications equipment  
should be used no closer to any  
part of the Grafco Ultrasound  
Pocket Doppler, including  
61000-4-3 GHz  
cables, than the recommended  
separation distance calculated  
from the equation applicable to  
the frequency of the transmitter.  
Recommended separation  
distance  
80 MHz to  
800 MHz  
800 MHz to  
2.5 GHz  
Where P is the maximum output  
power rating of the transmitter  
in watts (W) according to the  
transmitter manufacturer and d  
is the recommended separation  
distance in meters (m).  
Field strengths from fixed RF  
transmitters, as determined  
by an electromagnetic site  
survey,a should be less than  
the compliance level in each  
frequency range.b  
Interference may occur in the  
vicinity of equipment marked  
with the following symbol:  
14423-INS-LAB-RevD11  
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Info 1: At 80 MHz and 800 MHz, the higher frequency range applies.  
Info 2: These guidelines may not apply in all situations. Electromagnetic  
propagation is affected by absorption and reflection from struc-  
tures, objects and people.  
a: Field strengths from fixed transmitters, such as base stations for radio  
(cellular/cordless) telephones and land mobile radios, amateur radio, AM  
and FM radio broadcast and TV broadcast cannot be predicted theoreti-  
cally with accuracy. To assess the electromagnetic environment due to  
fixed RF transmitters, an electromagnetic site survey should be consid-  
ered. If the measured field strength in the location in which the Grafco  
Ultrasound Pocket Doppler is used exceeds the applicable RF compli-  
ance level above, the Grafco Ultrasound Pocket Doppler should be ob-  
served to verify normal operation. If abnormal performance is observed,  
additional measures may be necessary, such as reorienting or relocating  
the Grafco Ultrasound Pocket Doppler.  
b: Over the frequency range 150 kHz to 80 MHz, field strengths should  
be less than 3 V/m.  
Recommended Separation Distances  
Recommended separation distances between portable  
and mobile RF communications equipment and the Grafco  
Ultrasound Pocket Doppler  
The Grafco Ultrasound Pocket Doppler is intended for use in an  
electromagnetic environment in which radiated RF disturbances are  
controlled. The customer or the user of the device can help prevent  
electromagnetic interference by maintaining a minimum distance between  
portable and mobile RF communications equipment (transmitters) and the  
Grafco Ultrasound Pocket Doppler as recommended below, according to the  
maximum output power of the communications equipment.  
Rated  
maximum  
output power  
of transmitter  
(W)  
Separation distance according to  
frequency of transmitter (m)  
80 MHz to 800 MHz  
800 MHz to 2.5 GHz  
0.01  
0.1  
1
0.1167  
0.3689  
1.1667  
3.6893  
11.6667  
0.2334  
0.7378  
2.3334  
7.3786  
23.3334  
10  
100  
14423-INS-LAB-RevD11  
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For transmitters rated at a maximum output power not listed previously,  
the recommended separation distances in meters (m) can be estimated  
using the equation applicable to the frequency of the transmitter, where  
P is the maximum output power rating of the transmitter in watts (W)  
according to the transmitter manufacturer.  
Info 1: At 80 MHz and 800 MHz, the separation distance for the higher  
frequency range applies.  
Info 2: These guidelines may not apply in all situations. Electromagnetic  
propagation is affected by absorption and reflection from struc-  
tures, objects and people.  
14423-INS-LAB-RevD11  
39  
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12 APPENDIX C, OVERALL SENSITIVITY  
Overall Sensitivity (2 MHz Probe)  
Diameter Distance Reflection  
Two-way Attenuation B=∑Ba+Bw  
of  
(d)  
Loss A  
(d)  
Target  
Reflector  
(mm)  
(mm)  
∑Ba  
Bw  
(dB)  
B
(dB)  
(T:mm  
20 4.8 4.0  
Ba 40 9.6 8.0  
20 4.8 3.4  
Ba 40 9.6 6.8  
20 4.8 3.4  
Ba 40 9.6 6.8  
Ba:dB)  
1.58  
50  
45.7  
T
-
-
-
-
-
-
-
-
0
57.6  
56.4  
56.4  
49.6  
60.8  
58.4  
56.4  
51.6  
A=45.7dB  
@2 MHz  
75  
45.7  
45.7  
45.7  
43.2  
43.2  
43.2  
43.2  
T
0
0
0
0
0
0
0
100  
200  
50  
T
T
20 4.8  
-
-
Ba 40 9.6  
2.38  
A=43.2dB  
@2 MHz  
T
20 4.8 3.4 2.2  
Ba 40 9.6 6.8 4.4  
75  
T
20 4.8 3.4  
Ba 40 9.6 6.8  
20 4.8 3.4  
Ba 40 9.6 6.8  
1
2
-
100  
200  
T
-
T
20 4.8  
1
2
-
Ba 40 9.6  
-
Doppler 333  
Frequency  
(Hz)  
14423-INS-LAB-RevD11  
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Overall Sensitivity (2 MHz Probe)  
Diameter  
of  
Target  
Reflector  
(mm)  
Vn  
(r.m.s.) (r.m.s.)  
mV mV  
Vn  
Overall  
Sensitivity  
(S=A(d)+B+C)  
dB  
dB  
1.58  
A=45.7dB  
@2 MHz  
186  
94  
5.93  
5.78  
5.82  
5.68  
109.2  
107.8  
107.9  
100.9  
175  
174  
173  
90  
89  
90  
2.38  
A=43.2dB  
@2 MHz  
178  
170  
165  
160  
89  
90  
85  
85  
6.02  
5.52  
5.76  
5.49  
110.0  
107.1  
105.3  
100.2  
Doppler Velocity of Target 12.5  
Frequency (cm/s)  
(Hz)  
14423-INS-LAB-RevD11  
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13 INDEX  
A
Introduction 3  
Accessory equipment, certifica-  
tion of 6  
Appendix A, EC Declaration of  
Conformity 35  
Appendix C, Overall Sensitivity  
40  
L
Left panel features and illustra-  
tion 16  
M
Maintenance 25  
N
NOTICE statement, significance  
5
O
B
Operation 20  
Battery, installing / replacing 18  
P
Pocket Doppler, handling 10  
Pocket Doppler, inspection 11  
Pocket Doppler, intended use 3  
Pocket Doppler, storage 11  
Pocket Doppler, turning off 24  
Pocket Doppler, turning on 21  
Pocket Doppler, unpacking 10  
Pocket Doppler and accessories  
12  
Probe, FH monitoring with 22  
Probe, placing in the Pocket Dop-  
pler 20  
C
CAUTION statement, significance  
5
Cleaning 26  
D
Display panel 12  
E
Electromagnetic emissions—for  
all equipment and systems  
Electromagnetic immunity—for all  
equipment and systems (Ap-  
Electromagnetic immunity—for all  
equipment and systems that  
are not life-supporting (Ap-  
pendix B) 37  
Probe, removing from the Pocket  
Doppler 20  
Probe, swapping 21  
Probe operation 20  
Probes, vascular 17  
F
Probe socket 13  
Fetal Heart (FH) monitoring 22  
Freight policy, GF Health Prod-  
Front panel features and illustra-  
tion 12  
R
Rear panel features and illustra-  
tion 13  
Recommended separation dis-  
tances (Appendix B) 38  
G
S
Guidance and manufacturer’s  
Safety information 5  
Specifications 29  
START/STOP button 16  
I
Info statement, significance 5  
14423-INS-LAB-RevD11  
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T
Telephone number, Graham-Field  
Top panel features and illustra-  
tion 15  
U
User manual, contents of 3  
V
Volume control 16  
W
WARNING statement, signifi-  
cance 5  
14423-INS-LAB-RevD11  
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USA Corporate Headquarters:  
GF Health Products, Inc.  
2935 Northeast Parkway  
Atlanta, Georgia 30360  
telephone: 770-368-4700  
14423-INS-LAB-RevD11  
© 2011 GF Health Products, Inc.  
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