When Using Disposable Cuffs or YP-960T series Reusable Cuffs To use these NIBP cuffs, an optional YN-990P extension hose (1.5 m) is required. NOTE Connect the joints properly. If there is an air leak, NIBP cannot be measured properly. 1. Connect the NIBP cuff to the extension hose. 2. Connect the other end of the extension hose to the NIBP socket on the transmitter. Turn the joint clockwise until it clicks. To disconnect the cuff from the transmitter, turn the hose joint counterclockwise.
CAUTION NIBP and SpO2 can be measured on the same limb, but the SpO2 monitoring might not be accurate during NIBP measurement. Be careful when reading the SpO2 values.* * Monitoring SpO2 during NIBP Measurement When the SpO2 probe is attached to the same limb as the NIBP cuff, the blood flow decreases during NIBP measurement and pulse wave cannot be detected and SpO2 cannot be monitored properly.
Attaching the Transmitter on an Arm (Using the YP-943P/944P NIBP Cuff) 1. Attach the NIBP cuff to the transmitter. Refer to the “Connecting the NIBP Cuff to the Transmitter” section. 2. Insert the end of the cuff into the belt and then through the D ring as shown at left. Belt D ring End of cuff 3. Fold back the cuff at the D ring and fasten it using the velcro tape. Make sure that the cuff is not attached on a joint. NOTE The cuff must not wrap around the elbow.
Attaching the Strap to the Transmitter NOTE • Use the strap to prevent the transmitter from falling. • Do not attach the clip to hard objects such as thick cloth or zipper. It will break the clip. Attach a strap provided with the transmitter to the NIBP cuff and patient clothes. To open the clip, firmly pull out the tab in direction of the arrow. Belt for the strap on the NIBP cuff To adjust the strap length, push down the tab on the adjuster and slide. 1. Adjust the length of the strap. 2.
Placing the Transmitter on the Bed (Using the Disposable Cuffs or YP-960T series Reusable Cuffs) ARTERY ▼ 1. Put the cuff on the upper arm so that the ▼ mark of “ARTERY ▼” aligns with the artery of the patient. 2. Wrap the cuff so that “INDEX within the “ RANGE ”. RANGE ” comes If “Index ” is not within the “ ”, change the cuff size. RANGE Attaching Electrodes Selecting Electrode Lead CAUTION Only use Nihon Kohden specified electrodes and electrode leads.
Connecting the Electrode Lead to the Transmitter Connect the electrode lead to the ECG/RESP socket on the transmitter. When the transmitter is attached on an arm CAUTION CAUTION Do not shake or swing the transmitter while holding the leads or cables connected to the transmitter. The transmitter may come off and injure someone or damage surrounding instruments. Hold the connector of the electrode lead when connecting/disconnecting the electrode lead.
Six Electrodes The 6-electrode method with lead II and lead V5 is effective for monitoring myocardial ischemia. You can improve monitoring accuracy considerably by adding lead V4 to this combination. Va and Vb can be at any position of the standard 12 leads V1 to V6, but V4 and V5 are most appropriate for myocardial ischemic monitoring.
Lead Position Standard limb leads Lead I RA Lead II LA Lead III RA LL N (RL) Monopolar limb leads aVR lead N (RL) aVL lead aVF lead RA LA RA LA N (RL) N (RL) LA LL LL LL LA LL LL N (RL) RA RA LA N (RL) Monopolar chest leads V1 to V6 leads to RA LA LL N (RL) 48 Operator’s Manual ZM-940PA/941PA
Three Electrodes • Lead MII, which is similar to standard lead II, used when ECG measurement has priority Electrode Position Left infraclavicular fossa Right infraclavicular fossa Below lowest rib on the left anterior axillary line • Lead MI, which is similar to standard lead I Change F/LL and L/LA of the lead MII. Symbol AHA IEC LA L RA R LL F Lead Color AHA IEC Black Yellow White Red Red Green • Lead MIII, which is similar to standard lead III. Change R/RA and L/LA of the lead MII.
Attaching Electrodes to the Patient and Connecting the Electrode Leads to Disposable Electrodes Prepare the Patient Skin Shave off excessive body hair. To reduce skin impedance, clean the electrode site with cream or with a cotton pad moistened with alcohol. Thoroughly dry the skin with a clean cotton pad. NOTE • For a patient with frequent body movement, rub the sites with Skinpure skin preparation gel. However, do not use Skinpure skin preparation gel on sensitive skin.
Electrode Position for Respiration Monitoring Place the R/RA and F/LL electrodes so that the lungs are between the electrodes. NOTE The optimum electrode positions for ECG measurement of a patient are not always optimum for respiration measurement of the patient. Select positions suitable for both ECG and respiration measurements, or positions which have priority for one measurement. Electrode Position Examples NOTE The following examples are when monitoring with 3 electrodes.
Position 3 In this position, the respiration waveform is optimum, but the ECG lead is unusual. R or RA Right midaxillary at the horizontal level of V4 F or LL Fifth intercostal space on the left midaxillary line, V6 Position 4 In this position, the respiration measurement is influenced by the impedance variation of the abdomen, so the cardiac pulse wave included in the respiration wave is reduced.
Attaching the SpO2 Probe Selecting the SpO2 Probe Select an appropriate probe for the patient. CAUTION CAUTION Only use Nihon Kohden specified electrodes, electrode leads, SpO2 probes, and NIBP cuffs. Otherwise, the maximum performance from the transmitter cannot be guaranteed. Do not use a damaged or disassembled probe. It causes incorrect measurement and may injure the patient. Reusable Probes When using a TL-201T finger probe, choose the appropriate cable length for attachment.
Disposable Probes CAUTION The disposable probe is not sterilized. Use the disposable probe only for a single patient. Never reuse the disposable probe for another patient because it causes cross infection.
Probe TL-271T/TL-271T3 Cable length TL-271T: 0.8 m TL-271T3: 1.6 m TL-272T/TL-272T3 Cable length TL-272T: 0.8 m TL-272T3: 1.6 m TL-273T/TL-273T3 Patient Adult 30 kg or more Attachment Site Finger or toe Child 10 to 50 kg Neonate 3 kg or less Instep and sole Adult 40 kg or more Finger or toe Cable length TL-273T: 0.8 m TL-273T3: 1.6 m TL-274T/TL-274T3 Infant 3 to 20 kg Cable length TL-274T: 0.8 m TL-274T3: 1.
Connecting the SpO2 Probe to the Transmitter Connect the probe to the SpO2 socket on the transmitter. When the transmitter is attached on an arm 56 CAUTION CAUTION Do not shake or swing the transmitter while holding the leads or cables connected to the transmitter. The transmitter may come off and injure someone or damage surrounding instruments. Hold the connector when connecting/ disconnecting the SpO2 probe. If you disconnect the SpO2 probe by pulling the cable, it damages the cable.
Attaching the Probe to the Patient Attach the probe to the patient by referring to the probe’s manual. Make sure that the light emitter and photo detector of the probe face each other at the attachment site. WARNING WARNING • When using the TL-201T finger probe, do not fasten the probe and cable to the finger by wrapping with tape. This may cause burn, congestion or pressure necrosis from poor blood circulation.
CAUTION If the attachment site is dirty with blood or bodily fluids, clean the attachment site before attaching the probe. If there is nail polish on the attachment site, remove the polish. Otherwise, the amount of transmitted light decreases, and measured value may be incorrect or measurement cannot be performed. CAUTION If the skin gets irritated or redness appears on the skin from the probe, change the attachment site or stop using the probe. Take extreme care for the patients with delicate skin.
Locking the Keys on the Transmitter To prevent the patient from pressing the keys on the transmitter during monitoring, you can lock the NIBP START/STOP and NIBP INTERVAL keys. 1. Press the NIBP INTERVAL key for about 3 seconds. 2. A “pip, pip” sounds and the “LOCK KEYS” message is displayed on the LCD. Pip, pip LOCK KEYS When the NIBP START/STOP key or NIBP INTERVAL key is pressed while the keys are locked, the “PRESS INT. KEY 3S TO UNLOCK” message appears. To unlock the keys: 1.
Monitoring When preparation is done, monitoring starts. NIBP Oscillometric Method NIBP is measured from the change in amplitude pattern of pulsatile oscillation in cuff pressure as the cuff pressure is reduced from above systolic to below diastolic pressure. The occlusiveoscillometry method uses this to determine the systolic, diastolic and mean arterial pressure. NIBP Monitoring Selecting the Initial Cuff Inflation Pressure The initial cuff inflation pressure can be changed on the PARAMETER SETUP screen.
Refer to the “Changing Parameter Setup Settings” section. The STAT measurement completes within 15 minutes. When more than 12 minutes elapse from the start of measurement, there will be no more measurement performed and the measurement mode changes to the mode selected for “NIBP MODE AFTER STAT” on the PARAMETER SETUP screen. Auto Measurement In Auto mode, measurement is performed automatically at the preset time intervals.
NOTE • When measuring patients who are conscious, help the patient to relax. Measurement may not be accurate if the patient’s arm is tense or if the patient talks. • The data for measurement on a leg tends to be higher than measurement on the arm. When making diagnosis based on the NIBP values, measure NIBP on an upper arm. • Do not apply pressure to the cuff or air hose. NIBP may not be measured correctly because of noise or NIBP measurement may stop due to the NIBP safety circuit.
The cuff is inflated and the inflation pressure is displayed on the screen. Inflation pressure In manual mode: Measurement is performed once. In STAT mode: Measurement is performed repeatedly for 15 minutes. In auto mode: The first measurement is performed when the NIBP START/STOP key is pressed. The second measurement is performed when the current time in the transmitter reaches the selected time interval. To stop measurement during measurement, press the NIBP START/STOP key again.
Data Display After NIBP Measurement When the time set at “OLD NIBP DATA” on the PARAMETER SETUP screen elapses after the last measurement, the NIBP data is dimmed or hidden. Whether to dim or hide the old data can also be selected at “OLD NIBP DATA”. Refer to the “Changing Parameter Setup Settings” section. Data Display on the Receiving Monitor When the “Low battery ” message is displayed on the receiving monitor, NIBP might not have been measured according to the NIBP interval setting.
WARNING Interaction Between Minute Ventilation Rate-Adaptive Pacemakers and Cardiac Monitoring and Diagnostic Equipment* The bioelectric impedance measurement sensor of a minute ventilation rate-adaptive implantable pacemaker may be affected by transmitter which is connected to the same patient. If this occurs, the pacemaker may pace at its maximum rate and the transmitter may give incorrect data to the monitor.
patient. Pacing pulse is detected by the transmitter and transmitted to the monitor. If the pacing spike detection is turned OFF, QRS and pacemaker spike may not be distinguished and pacemaker failure may not be recognized. Electrode Detachment In the following conditions, the check electrode indication is displayed on the LCD of the transmitter and the “CHECK ELECTRODE” message is displayed on the monitor. • Electrode is detached from skin. • Electrode lead is disconnected from the electrode.
SpO2 Monitoring When monitoring starts, SpO2 and pulse waveform are sent to the monitor and SpO2, pulse rate and pulse level bar graph are displayed on the transmitter LCD. WARNING WARNING SpO2 measurement may be incorrect in the following cases. • When the patient’s carboxyhemoglobin or methemoglobin increases abnormally. • When dye is injected in the blood. • When using an electrosurgical unit. • During CPR. • When measuring at a site with venous pulse. • When there is body movement.
CAUTION CAUTION Turn off the power of mobile phones, small wireless devices and other devices which produce strong electromagnetic interference around a patient (except for devices allowed by the hospital administrator). Radio waves from devices such as mobile phones or small wireless devices may be mistaken as pulse waves and the displayed data may be incorrect. Do not pull or bend the probe cable, and do not put caster feet on the probe cable.
Monitoring SpO2 during NIBP Measurement When the SpO2 probe is attached to the same limb as the NIBP cuff, the blood flow decreases during NIBP measurement and pulse wave cannot be detected and SpO2 cannot be monitored properly. When “INHIBIT SpO2 DURING NIBP” on the PARAMETER SETUP screen is set to ON (factory default setting), SpO2 monitoring is paused during NIBP measurement to avoid SpO2 alarm occurrence. However, when monitoring SpO2 on the same limb as NIBP, be careful when reading SpO2 values.
Display and Message List Battery Indication Indication Cause Countermeasure Fully charged battery —— Batteries are low. Batteries are low. NIBP cannot be measured. No indication Replace batteries. Dead batteries ECG/Respiration Indication Cause Electrode lead is disconnected from the electrode. Electrode lead is disconnected from the transmitter. Electrode lead discontinuity. Electrode is not firmly attached to the skin. Polarization voltage is abnormally high.
SpO2 Message During NIBP measurement Cause SpO2 monitoring is paused for NIBP measurement. Considerable body movement. Detecting body The probe is not attached to the movement patient properly. The probe is not attached to the patient properly. SpO2 CHECK The probe is not attached at the PROBE appropriate site. Probe is expired. SpO2 DETECTING PULSE SpO2 LIGHT INTERFERENCE SpO2 PROBE FAILURE SpO2 WEAK PULSE Searching for the correct pulse wave.
NIBP Message Cause The cuff and extension hose are not properly connected. NIBP AIR LEAK The cuff hose (or extension hose) is not properly connected to the NIBP socket. Countermeasure Connect them properly. The cuff or extension hose is damaged. Replace with a new one. The patient’s pulse wave is small. Measure by palpation or auscultation. The cuff is not wrapped on the patient properly. Wrap the cuff on the patient properly.
Troubleshooting If the problem still remains after checking the following, contact your Nihon Kohden representative. Transmitter Problem Nothing is displayed on the LCD after turning the power on. Cause Batteries are not installed correctly. The battery polarity is wrong. Batteries are completely discharged. LCD is difficult to see LCD brightness is not (too dark or too light). appropriate. Nothing is displayed on the monitor after turning the transmitter power on. Signal receiving condition is poor.
ECG/Respiration Problem The heart rate is unstable. The “CHECK ELECTRODE” message appears on the receiving monitor. ECG baseline is thick. (Hum is overlapping) Respiration waveform measurement is unstable. Cause Countermeasure Pacing detection setting on the monitor is not correct. Turn off the pacing detection setting on the monitor. When monitoring a pacemaker patient, turn on pacing detection. Electrode lead is disconnected Firmly connect the electrode lead to the from the electrode. electrode.
NIBP Problem Cause Cuff inflation pressure The cuff hose is not connected is less than 10 mmHg. to the NIBP socket properly. The cuff is not wrapped around the arm or is wrapped too loosely. The cuff does not The cuff hose is not connected inflate when the NIBP to the NIBP socket. START/STOP key is The cuff hose or extension hose pressed. may be folded or squeezed when the cuff pressure display on the screen increases quickly but the actual cuff does not inflate. Abnormal The cuff size is not correct.
Problem Cause Cannot measure NIBP. Vibration on the cuff. Countermeasure Check that nothing is touching the cuff during measurement. The cuff hose or extension hose Remove the cause. is bent or squeezed. The cuff has worn out. Use a new cuff. Blood congestion Measuring over a long period of Increase the measuring interval. occurs. time at short intervals. Do not measure NIBP over a long time. Thrombus occurs.
Maintenance To use the instrument in safe and optimum condition, perform maintenance check once every six months. CAUTION Never disassemble or repair the transmitter. Disassembly and repair must be performed by qualified service personnel. A maintenance check sheet is provided at the end of this section. Make a copy of this check sheet before performing maintenance check. 1. External Check • There are no damaged or dirty parts on the outside of the transmitter.
3. While pressing the NIBP START/STOP and NIBP INTERVAL keys, install the battery. The SETUP screen appears. 4. Press the NIBP INTERVAL key to move the cursor to “SYSTEM SETUP”. 5. Press the NIBP START/STOP key to enter the SYSTEM SETUP screen. The channel of this transmitter is displayed. Channel 78 6. Check that the channel displayed on the LCD matches the label on the transmitter.
3. LCD Display Check that there are no dots missing on the LCD. 1. Remove one battery. 2. While pressing the NIBP START/STOP and NIBP INTERVAL keys, install the battery. The SETUP screen appears. 3. Press the NIBP INTERVAL key twice to move the cursor to “MANUAL CHECK”. 4. Press the NIBP START/STOP key to enter the MANUAL CHECK screen. 5. Check that the cursor is on “LCD TEST” and press the NIBP START/STOP key.
6. Every time the NIBP INTERVAL key is pressed, the screen changes as below. Check that there are no dots missing. When the NIBP START/STOP key is pressed, the screen returns to the MANUAL CHECK screen. 4. Key Operation NIBP START/STOP Key 1. Attach the NIBP cuff to your upper arm. 2. Press the NIBP START/STOP key. Check that the cuff inflates and deflates properly. 3. Press the NIBP START/STOP key again. During inflation, press the NIBP START/STOP key to check that the cuff deflates properly.
5. NIBP Cuff for Attaching Transmitter to Patient Arm The NIBP cuff is a consumable. Check the following and when necessary, replace it with a new one. Appearance • There are no dirty parts. • There are no broken stitches on the cuff. • The label on the cuff is readable. • The velcro tape on the cuff is not removed and there are no broken stitches. • The lock plate is not damaged and functions properly. Inflation bag • The inflation bag is not torn or damaged. • There is no water inside the inflation bag.
Maintenance Check Sheet Hospital/Organization: Service Personnel: Instrument Name: Transmitter Instrument Model: ZM-940PA/ZM-941PA Instrument Serial Number: Hardware Revision Number: Software Revision Number: 1. External Check OK No 2. Transmitter Channel OK No 3. LCD Display OK No 4. Key Operation OK No 5. NIBP Cuff for Attaching Transmitter to Patient Arm OK No Overall Judgement □ OK □ Can be used but needs maintenance □ Maintenance required. Cannot be used.
Repair Parts Availability Policy Nihon Kohden Corporation (NKC) shall stock repair parts (parts necessary to maintain the performance of the instrument) for a period of 8 years from the date of delivery. In that period NKC or its authorized agents will repair the instrument. This period may be shorter than 8 years if the board or part necessary for the faulty section is not available.
Lifetime and Disposal Disposing of Used Batteries Battery Lifetime Replace the batteries when the battery replacement indication appears on the transmitter. When using rechargeable batteries, recharge them. ZM-940PA Type NiMH secondary Alkaline primary Lifetime (Measuring parameters) ECG, SpO2, NIBP ECG, SpO2 ECG only 2 days 2.5 days 3 days 1 day 2.5 days 3 days ZM-941PA Type NiMH secondary Alkaline primary Lifetime (Measuring parameters) ECG, SpO2, NIBP ECG, SpO2 ECG only 1.5 days 2 days 2.
Cleaning, Disinfection and Sterilization Transmitter and Electrode Leads CAUTION CAUTION This transmitter is not waterproof. If detergent or liquid spills into the transmitter, stop cleaning or disinfecting it and contact your Nihon Kohden representative. The transmitter needs to be checked for safety and function before use. Before cleaning or disinfection, remove the batteries from the transmitter. Failure to follow this instruction may result in electrical shock or transmitter malfunction.
Disinfectant Glutaraldehyde solution Alkyldiaminoethylglycine hydrochloride Benzalkonium chloride Benzethonium chloride solution Chlorhexidine gluconate solution Concentration (%) 2.0 0.5 0.2 0.2 0.5 SpO2 Probe Refer to the probe manual. YP-943P/944P NIBP Cuffs CAUTION • • • • Do not autoclave. Use only glutaraldehyde solution. Never allow liquid to get inside the inflation bag. Do not sterilize or disinfect the cuff with ultraviolet light or ozone.
Specifications ZM-940PA Measuring Parameters Measuring waveforms: Measuring numeric data: ECG, Respiration in impedance method, pulse SpO2, NIBP, pulse rate Transmitting Data Waveform data: Numeric data: Status information: ECG, respiration, pulse wave SpO2 and NIBP Battery replacement, channel ID, type of transmitter, check electrodes, abnormal polarization voltage, pacing data, SpO2 status, NIBP status Displayed Data SpO2, NIBP, pulse rate, pulse wave bar graph, check electrode, battery replacement, N
When considering the measuring accuracy of the SpO2 probe: ±2 (80% ≤ SpO2 ≤ 100%) ±3 (70% ≤ SpO2 < 80%) Less than 70% is not specified NIBP Measurement Displayed items: Cuff pressure display range: Measurement modes: Measurement accuracy: Systolic, diastolic, mean 0 to 300 mmHg Manual, STAT, auto at 5, 10, 15, 30, 60, 120 or 240 minute interval ±3 mmHg (0 ≤ NIBP ≤ 200 mmHg) ±4 mmHg (200 < NIBP < 300 mmHg) Meets or exceeds AAMI Sp-10.
Battery lifetime: Type NiMH secondary Alkaline primary Lifetime (Measuring parameters) ECG, SpO2, NIBP ECG, SpO2 ECG only 2 days 2.5 days 3 days 1 day 2.5 days 3 days The above data is when the following batteries and battery charger which are recommended by Nihon Kohden are used. The measurement is performed at room temperature, NIBP is measured in auto mode at 60 minute intervals and SpO2 is measured on an index finger of a male patient with weight 60 kg.
IEC 60601-1 Amendment 2: 1995 IEC 60601-1-2: 2001 IEC 60601-2-27: 1994 IEC 60601-2-30: 1999 IEC 60601-2-49: 2001 According to the type of protection against electrical shock: INTERNALLY POWERED EQUIPMENT According to the degree of protection against electrical shock: ECG and impedance method respiration: DEFIBRILLATION-PROOF TYPE CF APPLIED PART SpO2 and NIBP: DEFIBRILLATION-PROOF TYPE BF APPLIED PART According to the degree of protection against harmful ingress of water: IPX0 (Ordinary equipment) A
Electromagnetic Immunity This Model ZM-940PA is intended for use in the electromagnetic environment specified below. The customer or the user of the ZM-940PA should assure that it is used in such an environment.
Immunity test IEC 60601 test level Compliance level Electromagnetic environment - guidance Portable and mobile RF communications equipment should be used no closer to any part of the ZM-940PA, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter. Recommended separation distance Conducted RF IEC 61000-4-6 3 Vrms 3 Vrms Radiated RF IEC 61000-4-3 3 V/m 3 V/m 80 MHz to 80 MHz to 2.5 GHz 2.5 GHz (1 V/m 80 MHz to 2.
Recommended Separation Distances between Portable and Mobile RF Communications Equipment The ZM-940PA is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the ZM-940PA can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the ZM-940PA as recommended below, according to the maximum output power of the communications.
ZM-941PA Measuring Parameters Measuring waveforms: Measuring numeric data: ECG, Respiration in impedance method, pulse SpO2, NIBP, pulse rate Transmitting Data Waveform data: Numeric data: Status information: ECG, respiration, pulse wave SpO2 and NIBP Battery replacement, channel ID, type of transmitter, check electrodes, abnormal polarization voltage, pacing data, SpO2 status, NIBP status Displayed Data SpO2, NIBP, pulse rate, pulse wave bar graph, check electrode, battery replacement, NIBP measurement
NIBP Measurement Displayed items: Cuff pressure display range: Measurement modes: Systolic, diastolic, mean 0 to 300 mmHg Manual, STAT, auto at 5, 10, 15, 30, 60, 120 or 240 minute interval ±3 mmHg (0 ≤ NIBP ≤ 200 mmHg) ±4 mmHg (200 < NIBP < 300 mmHg) Meets or exceeds AAMI Sp-10.
The above data is when the following batteries and battery charger which are recommended by Nihon Kohden are used. The measurement is performed at room temperature, NIBP is measured in auto mode at 60 minute intervals and SpO2 is measured on an index finger of a male patient with weight 60 kg. Operation time depends on the thickness of the SpO2 probe attachment site.
According to the type of protection against electrical shock: INTERNALLY POWERED EQUIPMENT According to the degree of protection against electrical shock: ECG and impedance method respiration: DEFIBRILLATION-PROOF TYPE CF APPLIED PART SpO2 and NIBP: DEFIBRILLATION-PROOF TYPE BF APPLIED PART According to the degree of protection against harmful ingress of water: IPX0 (Ordinary equipment) According to the degree of safety of application in the presence of a FLAMMABLE ANAESTHETIC MIXTURE WITH AIR, OR W
Electromagnetic Immunity This Model ZM-941PA is intended for use in the electromagnetic environment specified below. The customer or the user of the ZM-941PA should assure that it is used in such an environment.
Immunity test IEC 60601 test level Compliance level Electromagnetic environment - guidance Portable and mobile RF communications equipment should be used no closer to any part of the ZM-941PA, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter. Recommended separation distance Conducted RF IEC 61000-4-6 3 Vrms 3 Vrms Radiated RF IEC 61000-4-3 3 V/m 3 V/m 80 MHz to 80 MHz to 2.5 GHz 2.5 GHz (1 V/m 80 MHz to 2.
Recommended Separation Distances between Portable and Mobile RF Communications Equipment The ZM-941PA is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the ZM-941PA can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the ZM-941PA as recommended below, according to the maximum output power of the communications.
Standard Accessories 1 2 No. Name 1 NIBP cuff for adult, standard 2 Strap Model YP-943P — Q’ty 1 1 Supply Code No. S938B Y236 The following parts are available for replacement. 3 4 Lock plate is a standard accessory of the YP943P/944P NIBP cuff. No. Name 3 Battery case cover 4 Lock plate Model — — Operator’s Manual ZM-940PA/941PA Q’ty 1 1 Supply Code No.
Options CAUTION Only use Nihon Kohden specified electrodes, electrode leads, SpO2 probes, and NIBP cuffs. Otherwise, the maximum performance from the transmitter cannot be guaranteed. Transmitter Channel writer, QI-901PK ECG/RESP Name Electrode lead 102 Application 3 electrodes, clip type, lead length 80 cm 3 electrodes, snap type, lead length 80 cm 6 electrodes, clip type, lead length 80 cm 6 electrodes, snap type, lead length 80 cm Model Q’ty Supply Code No.
NIBP Width (cm) Name Cuff for adult, for attaching transmitter to patient arm Cuff for infant Cuff for child Cuff for adult Standard 13 Large 15 Small Standard Standard Large Disposable cuff for infant Disposable cuff for child Disposable cuff for adult Small Standard Medium large Large Extra large Extension hose 5 7 10 13 15 6 8 10 14 Air Hose Length (cm) 15 Model YP-943P* YP-944P* Q’ty 1 Supply Code No.
SpO2 Name Finger probe (reusable) Multi-site probe (reusable) Finger probe (reusable) SpO2 probe (for adult, disposable) SpO2 probe (for child, disposable) SpO2 probe (for neonate, disposable) SpO2 probe (for adult, disposable) SpO2 probe (for child, disposable) SpO2 probe (for neonate/adult, disposable) SpO2 probe (for child/infant, disposable) SpO2 probe (for adult/neonate, disposable) SpO2 probe (for child/infant, disposable) COTTONY tape Foam tape for TL-051S/052S/ 061S/062S Attachment tape for TL-220T/
Transmission Frequencies Channel: 9002 to 9478 Transmission Transmission Transmission frequency Channel No. frequency Channel No. frequency Channel No. (MHz) (MHz) (MHz) 608.0250 608.0375 608.0500 608.0625 608.0750 608.0875 608.1000 608.1125 608.1250 608.1375 608.1500 608.1625 608.1750 608.1875 608.2000 608.2125 608.2250 608.2375 608.2500 608.2625 608.2750 608.2875 608.3000 608.3125 608.3250 608.3375 608.3500 608.3625 608.3750 608.3875 608.4000 608.4125 608.
Transmission Transmission Transmission frequency Channel No. frequency Channel No. frequency Channel No. (MHz) (MHz) (MHz) 106 609.2625 609.2750 609.2875 609.3000 609.3125 609.3250 609.3375 609.3500 609.3625 609.3750 609.3875 609.4000 609.4125 609.4250 609.4375 609.4500 609.4625 609.4750 609.4875 609.5000 609.5125 609.5250 609.5375 609.5500 609.5625 609.5750 609.5875 609.6000 609.6125 609.
Transmission Transmission Transmission frequency Channel No. frequency Channel No. frequency Channel No. (MHz) (MHz) (MHz) 609.7000 9136 610.1500 9172 610.6000 9208 610.6125 9209 611.0625 9245 611.5125 9281 610.6250 9210 611.0750 9246 611.5250 9282 610.6375 610.6500 610.6625 610.6750 610.6875 610.7000 610.7125 610.7250 610.7375 610.7500 610.7625 610.7750 610.7875 610.8000 610.8125 610.8250 610.8375 610.8500 610.8625 610.8750 610.8875 610.9000 610.9125 610.9250 610.9375 610.9500 610.
Transmission Transmission Transmission frequency Channel No. frequency Channel No. frequency Channel No. (MHz) (MHz) (MHz) 108 611.0500 9244 611.5000 9280 611.9500 9316 611.9625 611.9750 611.9875 612.0000 612.0125 612.0250 612.0375 612.0500 612.0625 612.0750 612.0875 612.1000 612.1125 612.1250 612.1375 612.1500 612.1625 612.1750 612.1875 612.2000 612.2125 612.2250 612.2375 612.2500 612.2625 612.2750 612.2875 612.3000 612.3125 612.3250 612.3375 612.3500 612.3625 612.3750 612.
Transmission Transmission Transmission frequency Channel No. frequency Channel No. frequency Channel No. (MHz) (MHz) (MHz) 612.4000 9352 612.8500 9388 613.3000 9424 613.3125 9425 613.5375 9443 613.7625 9461 613.3250 9426 613.5500 9444 613.7750 9462 613.3375 9427 613.5625 9445 613.7875 9463 613.3500 9428 613.5750 9446 613.8000 9464 613.3625 9429 613.5875 9447 613.8125 9465 613.3750 9430 613.6000 9448 613.8250 9466 613.3875 9431 613.6125 9449 613.8375 9467 613.
Channel: E002 to E398 Transmission frequency (MHz) 1395.0250 1395.0375 1395.0500 1395.0625 1395.0750 1395.0875 1395.1000 1395.1125 1395.1250 1395.1375 1395.1500 1395.1625 1395.1750 1395.1875 1395.2000 1395.2125 1395.2250 1395.2375 1395.2500 1395.2625 1395.2750 1395.2875 1395.3000 1395.3125 1395.3250 1395.3375 1395.3500 1395.3625 1395.3750 1395.3875 1395.4000 1395.4125 1395.4250 1395.4375 1395.4500 110 Channel No.
Transmission frequency (MHz) 1396.3375 1396.3500 1396.3625 1396.3750 1396.3875 1396.4000 1396.4125 1396.4250 1396.4375 1396.4500 1396.4625 1396.4750 1396.4875 1396.5000 1396.5125 1396.5250 1396.5375 1396.5500 1396.5625 1396.5750 1396.5875 1396.6000 1396.6125 1396.6250 1396.6375 1396.6500 1396.6625 1396.6750 1396.6875 1396.7000 1396.7125 1396.7250 1396.7375 1396.7500 1396.7625 1396.7750 E107 E108 Transmission frequency (MHz) 1396.7875 1396.
Transmission frequency (MHz) Channel No. Transmission frequency (MHz) Channel No. 1397.6875 1397.7000 1397.7125 1397.7250 1397.7375 1397.7500 1397.7625 1397.7750 1397.7875 1397.8000 1397.8125 1397.8250 1397.8375 1397.8500 1397.8625 1397.8750 1397.8875 1397.9000 1397.9125 1397.9250 1397.9375 1397.9500 1397.9625 1397.9750 1397.9875 1398.0000 1398.0125 1398.0250 1398.0375 1398.0500 1398.0625 1398.0750 1398.
Transmission frequency (MHz) 1399.0375 1399.0500 1399.0625 1399.0750 1399.0875 1399.1000 1399.1125 1399.1250 1399.1375 1399.1500 1399.1625 1399.1750 1399.1875 1399.2000 1399.2125 1399.2250 1399.2375 1399.2500 1399.2625 1399.2750 1399.2875 1399.3000 1399.3125 1399.3250 1399.3375 1399.3500 1399.3625 1399.3750 1399.3875 1399.4000 1399.4125 1399.4250 1399.4375 1399.4500 E323 E324 Transmission frequency (MHz) 1399.4625 1399.
Channel: E502 to E898 Transmission frequency (MHz) 1427.0250 1427.0375 1427.0500 1427.0625 1427.0750 1427.0875 1427.1000 1427.1125 1427.1250 1427.1375 1427.1500 1427.1625 1427.1750 1427.1875 1427.2000 1427.2125 1427.2250 1427.2375 1427.2500 1427.2625 1427.2750 1427.2875 1427.3000 1427.3125 1427.3250 1427.3375 1427.3500 1427.3625 1427.3750 1427.3875 1427.4000 1427.4125 1427.4250 1427.
Transmission frequency (MHz) 1428.3000 1428.3125 1428.3250 1428.3375 1428.3500 1428.3625 1428.3750 1428.3875 1428.4000 1428.4125 1428.4250 1428.4375 1428.4500 1428.4625 1428.4750 1428.4875 1428.5000 1428.5125 1428.5250 1428.5375 1428.5500 1428.5625 1428.5750 1428.5875 1428.6000 1428.6125 1428.6250 1428.6375 1428.6500 1428.6625 1428.6750 1428.6875 1428.7000 1428.7125 1428.7250 1428.7375 E604 Transmission frequency (MHz) 1428.
Transmission frequency (MHz) 1429.6500 1429.6625 1429.6750 1429.6875 1429.7000 1429.7125 1429.7250 1429.7375 1429.7500 1429.7625 1429.7750 1429.7875 1429.8000 1429.8125 1429.8250 1429.8375 1429.8500 1429.8625 1429.8750 1429.8875 1429.9000 1429.9125 1429.9250 1429.9375 1429.9500 1429.9625 1429.9750 1429.9875 1430.0000 1430.0125 1430.0250 1430.0375 1430.0500 1430.0625 1430.0750 1430.0875 116 E712 E713 Transmission frequency (MHz) 1430.1000 1430.
Transmission frequency (MHz) 1431.0000 1431.0125 1431.0250 1431.0375 1431.0500 1431.0625 1431.0750 1431.0875 1431.1000 1431.1125 1431.1250 1431.1375 1431.1500 1431.1625 1431.1750 1431.1875 1431.2000 1431.2125 1431.2250 1431.2375 1431.2500 1431.2625 1431.2750 1431.2875 1431.3000 1431.3125 1431.3250 1431.3375 1431.3500 1431.3625 1431.3750 1431.3875 1431.4000 1431.4125 1431.4250 E820 E821 Transmission frequency (MHz) 1431.4375 1431.
