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        LifeDop 350 User Manual
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1.    17  Explanation of Symbols                                                    Back Cover    Please read the manual carefully and become familiar with the operation   features and maintenance of your LifeDop L350R prior to using the device  or accessories     EMERGO EUROPE    E C Molenstraat 15  0086 2513 BH  The Hague   This mark excludes the The Netherlands    Medichoice    model  MC350R     MANO0019 DFU    Rev  As 4 13 i Wallach Surgical Devices    Intended Use    Obstetric  2 and 3 MHz Probes   This product will be used to detect fetal heart beats as an aid for determining  fetal viability     Vascular  4  5 and 8 MHz Probes   This product will be used to detect blood flow in veins and arteries for  assisting in the detection of peripheral vascular disease     Caution     USS  Federal law restricts this device to sale by or on the order of a  licensed practitioner     Contraindications    Warnings     The vascular probes  4  5 and 8 MHz  are not for fetal use        The ultrasound probes are not to be used on or near the eyes      The device is for use only on intact skin        Do not plug any part of this device into a telephone or modem system   Any line connected accessory must meet applicable safety standards        This device is not intended for use with HF surgical equipment     If there are questions or concerns regarding these warnings or contraindications   please do not hesitate to contact Wallach Surgical Devices for further clarification     Caution     Dr
2.   watts per cm       MI the Mechanical Index   P  the peak rarefactional pressure  megapascals  associated with the transmit pattern  giving rise to the value reported for MI   Wo the total time average ultrasonic power  mwatts    f the probe center frequency  MHz    Zsp the axial distance at which the reported parameter is measured  cm    X6     6 are the  6dB beam dim  in the x y plane where Zs is found  cm    EBD the entrance beam dimensions  cm   These dimensions are the same as the  dimensions of the transmit crystal   Measurement Uncertainties  Power   34   42   Pressure   11   16   Intensity  Ispta    23   26   Frequency    5     Acoustic Output Parameters are measured in water  Derated values  denoted by the subscript     3     take into account a conservative level of attenuation that would be encountered in the  human body  The derated intensity values  13  are obtained from water values of intensity  Iw   at a depth of z calculated by     I    exp  0 23 0 3 f z  I    where f is the probe frequency in MHz and z is the depth in centimeters     The derated peak rarefactional pressure is calculated from the value of measure water  pr  by     P 3   exp  0 115 0 3 f z  p    where pressure is given in megapascals     Additional Output Reporting Information for IEC 61157       4 MHz  Lu  lt  91 mW cm    5 MHz  Lu  lt  51 mW cm   8 MHz  Lu  lt  47 mW cm      The 2 MHz  2 MHz WP and 3 MHz obstetrical probes are exempt from the declaration  requirements of IEC61157  These pro
3.  Devices for service     It is recommended that rechargeable batteries be replaced annually     MANO0019 DFU    Rev  A    4 13 10 Wallach Surgical Devices    Replacing Batteries    Warnings     Replace batteries only with batteries supplied by Wallach Surgical  Devices  See the Accessories section for reordering of parts information        The battery compartment only accepts AA size batteries  See the  Accessories section for reordering of parts information     Open the battery compartment by depressing the tab and pulling outward on  the battery door  Remove the existing drained batteries by pushing on the end  of the battery that compresses the battery contact spring and lift upwards  It is  acceptable to carefully use a simple tool  such as a pen  to assist in lifting out  the batteries     Battery Door Tab       Replace the batteries by paying close attention to the polarity indicators on the  battery and the polarity indicators on the battery holder in the compartment   Positive     aligns with positive  button  and negative     aligns with negative   spring   Insert the battery such that the spring contacts are loaded first and  then press the battery firmly into place  After all three have been inserted   replace the battery door     Warning       Ifthe batteries have been inserted incorrectly  the unit will not function  but the LifeDop 350 will not be damaged     MANO0019 DFU    Rev  A   4 13 11 Wallach Surgical Devices    Troubleshooting    Warning     Use alternat
4.  amp  Minor  Inc     Clorox    is a registered trademark of The Clorox Company        2013 Wallach Surgical Devices    WALLACH    SURGICAL DEVICES  95 Corporate Drive  Trumbull  CT 06611 USA  Phone  800 243 2463    203  799 2000  Fax   203  799 2002    customerservice wallachsurgical com  www wallachsurgical com    Made in the USA  MANO0019 DFU    Rev  Ae 4 13 Wallach Surgical Devices    
5.  for reordering of parts information        Do not attempt to recharge alkaline batteries  Otherwise  major  electrical damage is likely to occur     It is recommended that the LifeDop 350 be recharged prior to first use  To  recharge the unit  plug the recharge jack from the wall adaptor into the unit   s  recharge connector  The battery shaped indicator will cycle in a repeated  rising pattern to indicate the unit is recharging        Recharge jack from  power supply plugs  into connector  8 5 YDE  Z      The recharge cycle will be limited to 14 hours or until the maximum battery  voltage level has been reached  Once the recharge cycle has been discontinued  normally  the LCD indicator will flash at a low rate  The unit will not  overcharge the batteries  If it determines that the batteries do not require  charging  the charge cycle will be interrupted after 30 seconds     MANO0019 DFU    Rev  As 4 13 d Wallach Surgical Devices    Obtaining Doppler Signals    Caution     Doppler examinations should be performed only by trained individuals     For any Doppler examination  it is essential that an adequate supply of  coupling gel is used to transmit the ultrasound energy from the probe to the  surface of the skin  Re apply more gel if it starts to dry out or spread so  thinly that an air gap occurs between the probe and the skin  It is not  necessary to cover the entire surface of the probe  only the probe face   Applying too much gel makes the unit difficult to clean and does
6.  not aid in  the performance of the probe     Volume Control   The audio level can be adjusted using the Volume Slider  Slide the control  up toward the display to increase the volume  Slide the control back away  from the display to decrease it     Signal Quality Indicator   An inadequate signal can produce erroneous rates from the heart rate  calculation  The signal level that is being obtained is shown on the Signal  Quality Indicator bars  This indicator provides a visual aid in obtaining a  strong audio signal by showing the pulsatile nature of the signal  A large  difference between the highest and lowest signal bars that are lit confirms  that the quality of the signal is good and thus ensures the heart rate  calculation is operating at peak performance     The heart rate can be verified manually by counting the audible beats for  20 seconds and multiplying by 3  or for 15 seconds and then multiplying  by 4  Counting for less than 15 seconds is not recommended due to a  decrease in accuracy with the small sample size     Obstetrical   Fetal heart sounds are quite different from peripheral vascular blood flow  sounds  Fetal sounds are typically much lower in frequency and much  higher in rate  For early term fetal detection  start the probe at the pubic  bone and slowly move along the midline     rocking the probe slowly from  side to side until a heartbeat is heard  For mid to late term fetal detection  the best chance of finding the heart sounds are to start on the fu
7.  recharge        Recharge indicator off after charging  Battery level error has occurred     refer to Diagnostic Codes and contact service        Rechargeable unit does not hold a charge   Verify that the correct recharge adaptor is being used   Use only Wallach  Surgical Devices products    Batteries are old   Refer to Maintenance Section        MANO0019 DFU    Rev  Ae 4 13 12 Wallach Surgical Devices    Radio Frequency Interference   The LifeDop 350 family was tested for immunity to electromagnetic  interference at a level of 3 V meter  Interference during normal operation  may occur in the presence of fields stronger than 3 V meter  If this occurs   try to increase the distance between the LifeDop 350 and the source of  interference  Contact Wallach Surgical Devices for more information        Diagnostic Codes     Contact Wallach Surgical Devices    Service Dept                       1     Temperature too low 5    5 Volt Supply too low  2     Temperature too high 6    5 Volt Supply too high  3     Reference Voltage too low 7     Battery Voltage too low  4     Reference Voltage too high 8     Battery Voltage too high          Reference materials for Obstetrical and Peripheral Vascular testing     Handbook of Fetal Heart Rate Monitoring  Julian T  Parer  1997       Doppler Ultrasound and Its Use In Clinical Measurement  Peter Atkinson  and John P  Woodcock  1982       Noninvasive Diagnosis of Peripheral Vascular Disease  W  Robert Felix  Jr    1988       Current Noninvasive 
8. SummitDDppler     a WALLACH SURGICAL brand    User Manual for  LifeDop L350R Series  Tabletop Doppler        L350R  MC350R    WAILACH    SURGICAL DEVICES    C Eoose    MANO0019 DFU    Rev  As 4 13 Wallach Surgical Devices    Thank you for choosing LifeDop   L350 products  We believe you have  purchased the finest Doppler on the market today  Your total satisfaction is  our highest priority as we strive to continually improve our products and  services  Please contact us with any suggestions  We look forward to  enjoying a long term relationship with you     Wallach Surgical Devices  95 Corporate Drive  Trumbull  CT 06611 USA       Year of manufacture  located on the device     Here   s how you can reach us     Phone  1 800 243 2463   203  799 2000  Fax   203  799 2002  e mail us at  customerservice wallachsurgical com  visit our website at  www wallachsurgical com    Table of Contents     Page   Intended Use Contraindications WarningS                                1  Description Of Product                             aa    3  Operation and Installation                                                    5  Obtaining Doppler Signals a    8  Maintenance and Cleaning a    10  Replacing Batteries nn    11  Tro  blesh oti  g_            uu Eed EESEEEEE Se EENEG 12  Clinical References  uuu usun E 13  AN CCESSOTIES  ett rnain aiee ERE R EEEE  13  Specifications                                nn nasua    14  Warranty and Servicing Policy                                              
9. Vascular Diagnosis  Ali F  Aburahma  Edward B   Diethrich  1988       Accessories    To order accessories  gel  batteries  rechargers  stands  and probe cleaner    contact Wallach Surgical Devices at 1 800 243 2463 or  203  799 2000 to  order by phone     MANO0019 DFU    Rev  A    4 13 13 Wallach Surgical Devices    Specifications   Degree of protection against electric shock   A Type B Applied part  fei Class II Equipment    Degree of protection against ingress of water   IPX4     extending 2 5 cm from tip  IPX      entire probe 2 5 cm from tip  excluding connector    Designed and tested to meet   IEC601 1  IEC60601 1 2  IEC60601 2 37    Dimensions  h x w x l   200 x 150 x 100 mm  Weight  1000 grams   Operating temperature  10 to 40   C   Operating humidity  30 to 75    Transport Storage temperature     20 to 50   C  Transport Storage humidity  5 to 90   non condensing     beyond 30 days  battery to be stored between    20 and 30   C     Battery life  Batteries provided with LifeDop 350   5 hours continuous minimum  1000 1 minute exams typical    Battery type and voltage  3     AA NiMH 1 5 volt  rechargeable   Audio bandwidth and power  350 Hz     2 kHz  0 5 W  Heart rate calculation accuracy   3 BPM over range 50 to 220 BPM       Operating Conditions  There are no user controls which affect the  ultrasound output     A Attention  Consult Accompanying Documents    MANO0019 DFU    Rev  A    4 13 14 Wallach Surgical Devices    Transducer Model _LifeDop 4 MHz Operating Mode _Co
10. aging on return shipments to  Wallach Surgical Devices  improper maintenance or cleaning as described  in the user manual  misuse  abuse  alteration of the equipment from   its original specifications  or dismantling of the unit  other than by  Wallach Surgical Devices approved service technicians      Service Returns     To return products    1  Call Wallach Surgical Devices to obtain a Return Authorization and to  receive any final instructions prior to shipping    2  Clean the product prior to shipping    3  Ensure the device is well packaged and suitable for shipment     Send the product to   Repair Department  Wallach Surgical Devices  95 Corporate Drive  Trumbull  CT 06611 USA    For customer service  please call 1 800 243 2463 or  203  799 2000     MANO0019 DFU    Rev  Ae 4 13 17 Wallach Surgical Devices    Explanation of Symbols Se    Reorder Number a Keep Dry  D    S Serial Number  Type B Applied Part  Latex Free  ATTENTION     See instructions for use  IO Class II Equipment    E  gt    BE    Manufacturer     lt   2    Pd B    Date of Manufacture    Symbol indicates that the device should be sent to the special  agencies according to local regulations for separate collection after  its useful life     C    oose Product conforms to the Medical Device Directive 93 42 EEC      ec   rer   Authorized Representative in the European Community     LifeDop   Summit Doppler    and Wallach    are trademarks of CooperSurgical  Inc   Medichoice is a registered trademark of Owens 
11. and altered exposure conditions  It is therefore  considered appropriate to make the following recommendation     In those special situations in which examinations are to be carried out for  purposes other than direct medical benefit to the individual being examined   the subject should be informed of the anticipated exposure conditions  and of  how these compare with conditions for normal diagnostic practice     MANO0019 DFU    Rev  As 4 13 2 Wallach Surgical Devices    Description of Product    The LifeDop 350 is factory configurable to include many different features  and product enhancements  Along with user interchangeable ultrasound  transducers  the LifeDop 350 device is well suited to meet your specific  needs     Main Unit   The tabletop style main unit is ergonomically designed to be comfortable to  carry and allow easy access to each control feature  Each unit is individually  tested and inspected to ensure the highest quality standards     SSO     Superior Sound Quality  Every LifeDop 350 is designed with a state  of the art speaker sound system that produces excellent sound quality and  long term reliability     Recharge     We offer the ease of use of a rechargeable system or in some  limited areas a non rechargeable unit  Either way  the LifeDop 350 battery  system has been designed with your long term battery life needs in mind     LCD Display     The LCD display allows you to view the fetal or vascular  heart rate in larger  easy to read digits  monitor batte
12. bes meet the conditions  Io  lt  20 mW cm     Las  lt  100  mW cm     and P   lt  1 MPa  Io is output power divided by beam area     Note that parameter Zs in the probe reporting tables is the same parameter as I  in IEC 61157     MANO0019 DFU    Rev  As 4 13 16    Wallach Surgical Devices    Warranty and Servicing Policy    The warranty on this product is that it will be free from defects in material  and workmanship for 24 months from the original sale of the device   Product life is specified to be 5 years from manufacture  though the device  may be repairable beyond this timeframe  This includes all parts and labor  required to repair or replace the unit to original specifications and shipping  costs associated with sending the product back to the customer  Customer is  responsible for providing adequate packaging materials and shipping costs to  Wallach Surgical Devices  Products shall be repaired or replaced in a  reasonable amount of time     Wallach Surgical Devices    liability for any claim is limited to materials and  labor associated with repair or replacement  In no event shall Wallach  Surgical Devices be liable for incidental or consequential losses or damages  in connection with the purchase of this product     Wallach Surgical Devices disclaims all express or implied warranties   agreements or arrangements other than issued in this warranty     Wallach Surgical Devices is not responsible for damages to the device  that occur as a result of the inadequate pack
13. e equipment in case of unit failure  Call Wallach Surgical  Devices    Service Department if the probe or main unit malfunctions     Caution     Do not drop or mishandle the LifeDop 350  probes or accessories   Damage to sensitive electrical components  speakers  cables   transducers or plastic is likely to occur     Poor sound quality  Inadequate gel use    Try to relocate the probe for a better signal     refer to Signal Strength Indicator  Improper choice of probe Frequency   Interference from other equipment   Probe coiled cable or battery contacts may be intermittent   Debris in the speaker may cause poor sound   Device damage from dropping the LifeDop 350  probes or accessories    Heart Rate inaccurate   Try to relocate the probe for a better signal     refer to Signal Strength Indicator  For OB  ensure maternal sounds are not mixing with fetal sounds   Ensure by manual counting that the rate is between 50 and 220 BPM       Battery indicator flashing  Consult the Battery Monitoring section  replace batteries as described in the  Replacing Batteries section           Probe frequency does not match the connected probe   Check probe that is attached to ensure it is the correct one  or check to see if  probe is attached  If correct probe is being used  contact Wallach Surgical  Devices    Service Department     Error 5 or 7  Batteries are low  They require replacement or recharging     Recharge indicator flashing  Recharge cycle is complete or the batteries didn   t require
14. eaned and examined regularly per the following guidelines     After every examination    Excess gel should be wiped off prior to docking the probe  Probes and main  unit should be cleaned with a damp cloth using warm water or presaturated  isopropyl alcohol wipes  In particular  pay close attention to clean the seams  along the plastic lines at the probe face but do not allow water or spray to  enter through the connectors or speaker grill        To disinfect unit  use commercially available spray or wipe disinfectants  registered with the EPA  Clorox    Broad Spectrum Quaternary Disinfectant  is the only disinfectant that is Wallach Surgical Devices approved for use  with the 350 Series Products  Follow the manufacturer   s instructions and  wipe unit until it is dry of solutions  Examiners should wash hands and  change gloves after every exam  Refer to local and hospital policies for  cleaning and disinfection policies     Store unit in a clean area free from dust and debris  Follow temperature and  humidity guidelines as specified at the end of this manual     Warning     Ifthe unit is to be stored for longer than 90 days without use  remove  the batteries prior to storage     Periodically  at least annually     Inspect the main unit and probes for signs of cracks or breaks in the  mechanical housing  Inspect cables and connectors for signs of wear or  failure  The user should discontinue use of the unit with any sign of loss of  housing integrity  Contact Wallach Surgical
15. is  the higher the frequency of the sound     Peripheral venous sounds are not typically periodic and vary greatly  depending on patient movement and breathing  These sounds are more like  the wind at the ocean and vary in pitch as the patient moves or breathes     4 MHz Vascular   The use of the 4 MHz vascular probe is the same as the 8 MHz as described  above  except tilting the probe 45 degrees is not necessary since the crystals  are angled inside the probe cap  This allows the user to simply place the  probe flat on the peripheral vascular surface to scan for the flow sounds by  moving the flat probe face across the skin surface above the vessel     Proper alignment of  the 4 MHz vascular  probe with respect  to the vessel       MANO0019 DFU    Rev  A    4 13 9 Wallach Surgical Devices    Maintenance and Cleaning    Warnings     The LifeDop 350 is not designed for liquid immersion  Do not soak the  main unit or probes in liquids  Use only spray or wipe cleaners and  disinfectants  Do not use products containing bleach        The LifeDop 350 is not designed for sterilization processes such as  autoclaving  gamma radiation or hydrogen gas        The LifeDop 350 is not intended to be used on open skin  If there is  evidence of open wound contamination  disinfect the probe before  using again as described below     The LifeDop 350 requires very little maintenance  However  it is important  to continuing function of the unit and the health of the patients that the unit  is cl
16. ndus and  move toward the navel and from one side of the abdomen to the other   slowly rocking the probe until the heartbeat is heard  The fetal heart  reminds many people of a galloping horse and can vary in tone from a  distant swishing sound to a hard clopping sound depending on the position  of the baby and probe     MANO0019 DFU    Rev  Ae 4 13 8 Wallach Surgical Devices    Obstetrical  continued    Many times when attempting to detect the fetal heart  the maternal vascular  sounds are heard instead of  or in some cases  in addition to  the fetal  sounds  These maternal sounds can come from one of the major arteries   the placenta or the umbilical cord  The maternal vascular sounds are  typically higher in frequency at a lower rate  The heart rate calculation  will display either the maternal rate or the fetal rate  whichever portion of  the signal is stronger     If the fetal heart sounds cannot be located using the procedure as described  above  a second exam should be performed using another commercially  available fetal monitor as a repeated test     5 and 8 MHz Vascular   Peripheral arterial sounds are typically higher in frequency  For the best  sounds  angle the probe approximately 45 degrees from the skin surface over  the general location of the vessel  Slowly move the probe side to side and  vary the angle of the probe until the vascular sounds are heard  Changing  the angle of the probe has an effect on the frequency of the sound  The  steeper the probe angle 
17. nstruments   Although the possibility exists that such biological effects may be identified  in the future  current data indicate that the benefits to patients of the prudent  use of diagnostic ultrasound outweigh the risks  if any  that may be present     Prudent Use   Approved May 1999  The AIUM advocates the responsible use of diagnostic ultrasound  The  AIUM strongly discourages the non medical use of ultrasound for  psychosocial or entertainment purposes  The use of either two dimensional   2D  or three dimensional  3D  ultrasound to only view the fetus  obtain a  picture of the fetus or determine the fetal gender without a medical  indication is inappropriate and contrary to responsible medical practice   Although there are no confirmed biological effects on patients caused by  exposures from present diagnostic ultrasound instruments  the possibility  exists that such biological effects may be identified in the future  Thus  ultrasound should be used in a prudent manner to provide medical benefit to  the patient     Safety in Training and Research   Approved March 1997  March 1983  Diagnostic ultrasound has been in use since the late 1950s  There are no  confirmed adverse biological effects on patients resulting from this usage   Although no hazard has been identified that would preclude the prudent and  conservative use of diagnostic ultrasound in education and research   experience from normal diagnostic practice may or may not be relevant to  extended exposure times 
18. ntinuous Wave  cw   Application s  _ Peripheral Vascular    l l  acousncourrer Lu   omien   onien    Global Maximum Value  D   Mpa     Wo  mW                 Associated       Acoustic fo  MHz        Parameter  Zsp  cm        Se  cm   Ve  cm   Az  cm   Ele   cm        Beam Dimensions          EBD                Transducer Model _LifeDop 3 MHz Operating Mode _Continuous Wave  cw   Application s  _ Peripheral Vascular                 Global Maximum Value                                      D    pay  Associated   W   on  sone L  MHz  5 3  Parameter    Zsp  cm  0 85  xs Cm Winih       Beam Dimensions ys  cm     Az  cm                        Transducer Model _LifeDop 8 MHz Operating Mode _Continuous Wave  cw        Application s  _ Peripheral Vascular       Global Maximum Value  Pr3  Mpa   Associated   W    mW     Acoustic fo  MHz   Parameter                Zsp  cm        Xe  cm   Ve  cm   Az  cm   EBD Ele   em        Beam Dimensions                      MANO0019 DFU    Rev  As 4 13 15 Wallach Surgical Devices    Obstetrical Probe Information        Model Number                                     IsATA  max   W cm  19 6 17 0  P   mW  48 0 24 5  Effective Radiating Area Lem  2 45 1 57  Ultrasound Frequency  MHz  2 1 MHz 3 2 MHz  Pulse Duration CW CW  Repetition Freq  CW CW  Isara the spatial average temporal average intensity  mwatts per cm       Tspra3 the derated spatial peak temporal average intensity  mwatts per cm       Tsppa 3 the derated spatial peak pulse average intensity
19. on  the LifeDop 350 performs a series of diagnostic checks   The unit first checks and temporarily displays the frequency of the probe that  is being used  This display will not reappear unless the probe is changed or  the power is cycled  in which case the display will again temporarily confirm  the frequency of probe that is connected     The unit then checks for proper internal operating temperature  battery  voltage  reference voltage and power supply voltage levels  If any of these  characteristics are out of range  the display will show the ERROR indicator  and a failure code associated with the diagnostic error  Diagnostic functions  are periodically checked while the unit is on to ensure the LifeDop 350 is  operating at peak performance  Refer to the Troubleshooting section for a  listing of failure codes     MAN0019 DFU    Rev  A    4 13 6 Wallach Surgical Devices    Battery Monitoring   All LifeDop 350 units perform continuous battery monitoring and give a  visual indication of battery level  The display shows a multiple level  battery shaped indicator that indicates the voltage level of the battery    The battery outline will flash when the battery level is very low  indicating  that the user should change the batteries soon after the current examination  is complete     Recharging  Warnings     Do not use any other wall adaptor unit other than that supplied with the    LifeDop 350  Otherwise  major electrical damage is likely to occur   See the Accessories section
20. opping the LifeDop 350  probe or accessories may cause damage to  the housing or electronics     In order to preserve  protect and improve the quality of the  environment  protect human health and utilize natural resources  prudently and rationally     do not dispose of waste electrical or  electronic equipment  WEEE  as unsorted municipal waste   Contact local WEEE disposal sites     Safety of Ultrasound   LifeDop 350s were designed with physician and patient safety in mind  In  early design phases all potential hazards were eliminated or reduced to As  Low As Reasonably Achievable  ALARA  by adhering to good design  practices and industry wide safety standards  Ultrasound procedures should  be performed with the ALARA principle in mind when delivering ultrasound  energy into the body     MANO0019 DFU    Rev  A   4 13 1 Wallach Surgical Devices    The following official statements from the American Institute of Ultrasound  Medicine  AIUM  are provided for your general information regarding the  safe use of ultrasound     Clinical Safety  Approved March 1997  October 1982  Diagnostic ultrasound has been in use since the late 1950s  Given its known  benefits and recognized efficacy for medical diagnosis  including use during  human pregnancy  the American Institute of Ultrasound in Medicine herein  addresses the clinical safety of such use     There are no confirmed biological effects on patients or instrument operators  caused by exposures from present diagnostic ultrasound i
21. ry life and battery  recharging  and observe signal strength indicators  and provides multiple  diagnostic indicators that ensure your unit is functioning at peak  performance levels     MANO0019 DFU    Rev  As 4 13 3 Wallach Surgical Devices    Probes   LifeDop 350 ultrasound transducers were designed to meet your specific  applications needs  Each probe has been ergonomically designed for  comfort while providing excellent maneuverability for locating the fetus or  vascular target     Each probe is carefully measured and tested to ensure it meets exacting  performance standards     2 MHz   Late term obstetrical examination  This probe frequency is  typically used during the last trimester for deep fetal positions associated  with larger women  Waterproof versions of the 2 MHz probe are available     3 MHz     Early and general purpose obstetrical examination  This probe  frequency is a general use model ideal for most stages of fetal examination   Fetal heart sounds can be heard as early as 12 weeks and sometimes sooner  depending on the position and size of the fetus     4 MHz Broad     This unique peripheral vascular probe is ideal for quickly  locating brachial  radial and ankle arteries in the performance of  Ankle Brachial Index testing  The broad beam of the 4 MHz probe allows  the user to place the probe over the general location of the artery and with  very little movement find the vessel for fast blood pressure measurements     5 MHz     This standard    pencil    
22. style probe is an excellent vascular tool for  locating deep specific vessels in the peripheral vascular system  The narrow  grip and small face of the probe make it ideal for maneuvering for maximizing  the signal     8 MHz     This standard    pencil    style probe is an excellent vascular tool for  locating shallow specific vessels in the peripheral vascular system  The  narrow grip and small face of the probe make it ideal for maneuvering for  maximizing the signal     8 MHz Sterilizable     This vascular probe has a narrow beam for detection of  blood flow in both veins and arteries  It is validated for use in sterile fields     MANO0019 DFU    Rev  As 4 13 4 Wallach Surgical Devices    Operation and Installation    Probe Volume On Off Graphic  Holder Slider Display          Probe Recharge Headphone  Connector Connector Connector    MANO0019 DFU    Rev  Ae 4 13 5 Wallach Surgical Devices    HEART RATE       INDICATOR  BATTERY PROBE  VEUIRECHAR FREQUENCY    INDICATOR   INDICATOR  ERROR  INDICATOR  LAY  INDICATOR DIGIT  DISPLAY AREA  RECORD  INDICATOR SIGNAL QUALITY  INDICATOR  LCD Panel  Turning Unit On Off    Turn the unit on by pressing the On Off button  LCD indicators indicate  power status     The LifeDop 350 automatically shuts off after 3 minutes if it is not being  used  This complete power shutdown preserves the life of the batteries and  ensures the unit will be ready for operation in case it was accidentally left on     Diagnostic Monitoring   Once the unit is 
    
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