IPROVEN BPM-337 Series Blood Pressure Monitor Instruction Manual

IPROVEN BPM-337 Series Blood Pressure Monitor

Introduction

Thank you for making iProven your top choice. Please read the instructions carefully in order to accurately and safely utilize this equipment.

The BPM-337 measures the blood pressure and the heart rate and saves the results. The BPM-337 offers real time and accurate readings that are as convenient as possible thanks to the Oscillometric Measuring method. Blood pressure measurements may not be valid or accurate if they are not performed in accordance with the instructions provided in this manual. Please keep these instructions handy for future reference. You can also find the digital version of this manual on www.lproven.com

It is our passion to develop high quality products for home use. Our products are manufactured at the highest technical standards of professional quality, durability, and consistency. They are also designed with elegant simplicity in mind, making them easy to use at home.
To help you get the most from our products, we provide clear instructions with each device. The manual also includes helpful information that contributes to your overall health awareness.

In order to make sure that our products are tailored to your needs, we welcome your feedback. If you have any issues, questions or recommendations, please share your thoughts with us at www.iproven.com

Intended use of the BPM-337 Blood Pressure Monitor

The BPM-337 is a digital monitor that is used for measuring blood pressure and heart rate by cuffing the device around wrists of different sizes from 51/,–8½- (13.5cm to 21.5 cm). The BPM-337 is intended for home use and for adults only.

How This Device Works

The product uses the Oscillometric Measuring method to detect blood pressure. When the measurement is started, it calibrates to “zero pressure which Is the natural air pressure. As soon as It starts Inflating the wrist cuff, the device detects the pressure oscillations according to the beat-to-beat pulsatile and so It determines the systolic, diastolic pressure and the heart rate.

Irregular Heart Beat Detection

The device is equipped with irregular heart beat detection, IHB. The algorithm of the device compares the longest and shortest intervals of registered pulse waves (the time interval) and calculates the standard deviation. If the differences in the time intervals are more than 25% you have an irregular heartbeat and the IHB sign will appear in the display. If the device detects Irregular heartbeat during consecutive measurements and you are following the correct procedure, please consult your doctor.

Contraindications

1. The device is not suitable for use on the women who are or may be pregnant.
2. The device is not suitable for use on patients with implanted, electrical devices, such as cardiac pacemakers, defibrillators.

List of Accessories

• IProven model no, BPM-337
• 2* AAA alkaline batteries
• User manual

Cautions

• This device is intended for adult use in homes only.
• The device is not suitable for use on neonatal patients, pregnant women, patients with implanted, electronically devices, patients with preeclampsia, premature ventricular beats, atrial fibrillation, peripheral, arterial disease and patients undergoing intravascularly therapy or arteriovenous shunt or people who received a mastectomy. Please consult your doctor prior to using the unit if you suffer from illnesses.
• The device is not suitable for measuring the blood pressure of children. Ask your doctor before using it on older children.
• The device is not intended for patient transport outside a healthcare facility.
• The device is not intended for public use.
• This device is intended for no invasive measuring and monitoring of arterial blood pressure. It is not intended for use on extremities other than the wrist or for functions other than obtaining a blood pressure measurement.
• Do not confuse self-monitoring with self-diagnosis. This unit allows you to monitor your blood pressure. Do not begin or end medical treatment without asking a physician for treatment advice.
• If you are taking medication, consult your physician to determine the most appropriate time to measure your blood pressure. Never change a prescribed medication without consulting your physician.
• Do not take any therapeutic measures on the basis of a self measurement. Never alter the dose of a medicine prescribed by a doctor. Consult your doctor if you have any question about your blood pressure.
• When the device is used to measure patients who have common arrhythmias such as atrial or ventricular premature beats or atrial fibrillation, the best result may occur with deviation. Please consult your physician about the result.
• Don’t kink the connection tube during use, otherwise, the cuff pressure may continuously increase which can prevent blood flow and result in harmful injury to the PATIENT.
• When using this device, please pay attention to the following situation which may interrupt blood flow and influence blood circulation of the patient, thus cause harmful injury to the patient: connection tubing kinking too frequent and consecutive multiple measurements; the application of the cuff and its pressurization on any wrist where intravascular access or therapy, or an arteriovenous (A-V) shunt, is present; inflating the cuff on the side of a mastectomy.
• Warning : Do not apply the cuff over a wound; otherwise it can cause further injury.
• Do not inflate the cuff on the same limb which other monitoring ME equipment is applied around simultaneously, because this could cause temporary loss of function of those simultaneously used monitoring ME equipment.
• On the rare occasion of a fault causing the cuff to remain fully inflated during measurement, open the cuff immediately. Prolonged high pressure (cuff pressure ＞ 300mmHg or constant pressure ＞ 15mmHg for more than 3 minutes) applied to the wrist may lead to an ecchymosis.
• Please check that operation of the device does not result in prolonged impairment of patient blood circulation.
• When measuring, please avoid compression or restriction of the connection tubing.
• The device cannot be used with HF surgical equipment at the same time.
• The ACCOMPANYING DOCUMENT shall disclose that the SPHYGMOMANOMETER is clinically investigated according to the requirements of ISO 81060-2:2013.
• To verify the calibration of the AUTOMATED SPHYGMOMANOMETER, please contact the manufacturer.
• This device is contraindicated for any female who may be suspected of, or is pregnant. Besides providing inaccurate readings, the effects of this device on the fetus are unknown.
• Too frequent and consecutive measurements could cause disturbances in blood circulation and injuries.
• This unit is not suitable for continuous monitoring during medical emergencies or operations. Otherwise, the patient’s wrist and fingers will become anaesthetic, swollen and even purple due to a lack of blood.
• When not in use, store the device in a dry room and protect it against extreme moisture, heat, lint, dust and direct sunlight. Never place any heavy objects on the storage case.
• This device may be used only for the purpose described in this booklet. The manufacturer cannot be held liable for damage caused by incorrect application.
• This device comprises sensitive components and must be treated with caution. Observe the storage and operating conditions described in this booklet.
• The maximum temperature that the applied part can be achieved is 108.5°F (42.5°C) while the environmental temperature is 104°F (40°C).
• The equipment is not AP/APG equipment and not suitable for use in the presence of a flammable anesthetic mixture with air of with oxygen or nitrous oxide.
• Warning : No servicing/maintenance while the ME equipment is in use.
• The patient is an intended operator.
• The patient can measure data and change batteries under normal circumstances and maintain the device and its accessories according to the user manual.
• To avoid measurement errors, please avoid the condition of strong electromagnetic field radiated interference signal or electrical fast transient/burst signal.
• The blood pressure monitor and the cuff are suitable for use within the patient environment. If you are allergic to polyester, nylon or plastic, please don’t use this device.
• During use, the patient will be in contact with the cuff. The materials of the cuff have been tested and found to comply with requirements of ISO 10993-5:2009 and ISO 10993-10:2010. It will not cause any potential sensation or irritation reaction.
  • If you experience discomfort during a measurement, such as pain in the wrist or other complaints, press the START/STOP button to release the air immediately from the cuff. Loosen the cuff and remove it from your wrist.
  • If the cuff pressure reaches 40 kPa (300 mmHg), the unit will automatically deflate. Should the cuff not deflate when pressure reaches 40 kPa (300 mmHg), detach the cuff from the wrist and press the START/STOP button to stop inflation.
  • Before use, make sure the device functions safely and is in proper working condition. Check the device, do not use the device if it is damaged in any way. The continuous use of a damaged unit may cause injury, improper results, or serious danger.
  • Do not wash the cuff in a washing machine or dishwasher!
  • The service life of the cuff may vary by the frequency of washing, skin condition, and storage state. The typical service life is 10000 times.
  • It is recommended that the performance should be checked every 2 years and after maintenance and repair, by retesting at least the requirements in limits of the error of the cuff pressure indication and air leakage (testing at least at 50 mmHg and 200 mmHg).
  • Please dispose of ACCESSORIES, detachable parts, and the ME EQUIPMENT according to the local guidelines.
  • Manufacturer will make available on request circuit diagrams, component part lists, descriptions, calibration instructions, etc., to assist to service personnel in parts repair.
  • The operator shall not touch output of batteries and the patient simultaneously.
  • Cleaning :Dust environment may affect the performance of the unit. Please use the soft cloth to clean the whole unit before and after use. Don’t use any abrasive or volatile cleaners.
  • The device doesn’t need to be calibrated within two years of reliable service.
  • If you have any problems with this device, such as setting up, maintaining or using, please contact our customer service at [email protected]. Don’t open or repair the device by yourself in the event of malfunctions. The device must only be serviced, repaired and opened by individuals at authorized sales/service centers.
  • Please report to iProven if any unexpected operation or events occur.
  • Keep the unit out of reach of infants, young children or pets to avoid inhalation or swallowing of small parts. It is dangerous or even fatal.
  • Be careful to strangulation due to cables and hoses, particularly due to excessive length.
  • At least 30 min required for ME equipment to warm from the minimum storage temperature between uses until it is ready for intended use. At least 30 min required for ME equipment to cool from the maximum storage temperature between uses until it is ready for intended use.
  • This equipment needs to be installed and put into service in accordance with the information provided in the ACCOMPANYING DOCUMENTS;
  • Wireless communications equipment such as wireless home network devices, mobile phones, cordless telephones and their base stations, walkie-talkies can affect this equipment and should be kept at least a distance d away from the equipment. The distance d is calculated by the MANUFACTURER from the 80 MHz to 5.8 GHz column of Table 4 and Table 9 of IEC 60601-1-2:2014, as appropriate.
  • Please use ACCESSORIES and detachable parts specified/ authorised by MANUFACTURER. Otherwise, it may cause damage to the unit or danger to the user/patients.
  • There is no luer lock connectors are used in the construction of tubing. If there has, there is a possibility that they might be inadvertently connected to intravascular fluid systems, allowing air to be pumped into a blood vessel.
  • Please use the device under the environment which is provided in the user manual. Otherwise, the performance and lifetime of the device will be impacted and reduced.

Components Of The BPM-337

The Monitor Components

The LCD Display

during measurement.
| Error| See Error Message, and FAQ section
| Memory| indicating the memory mode and the number of the measurement
| Time| Hour Minute ( Month/Day/Year)
| Measurement units| Measurement unit of blood pressure ( 1 mmHg= 0.133 kpa)
| Average value| The average value of blood pressure

The Cuff Components

Component List:

1. PCBA
2. Air pipe
3. pump
4. Valve
5. Cuff
   

How To Install And Replace Batteries

1. Open the battery cover
2. Insert the two AAA batteries conform the right polarity
3. Close the battery cover
   

Tie the Cuff

1. Remove all accessories (watch, bracelet, etc) from your wrist. If your physician has diagnosed you with poor circulation in your wrist, use the other one.
2. Roll or push up your sleeve to expose the skin.
3. Apply the cuff to your wrist with your palm facing up.
4. Position the edge of the cuff about 0.4″ – 0.60″ (1 cm – 1.5 cm). from wrist joints.
5. Fasten the wrist cuff around your wrist, leaving no extra room between the cuff and your skin. If the cuff is too loose, the measurement will not be accurate.
6. Sit comfortably with your tested wrist resting on a flat surface. Place your elbow on a table so that the cuff is at the same level as your heart. Turn your palm upwards. Sit upright in a chair, and take 5-6 deep breaths.
7. Patients with Hypertension:
   The middle of the cuff should be at the level of the right atrium of the heart; Before starting measurement, please sit comfortably with legs uncrossed, feet flat on the floor, back and wrist supported.
   Rest for 5 minutes before measuring.
   Wait at least 3 minutes between measurements.
   This allows your blood circulation to recover.
   Take the measurement in a silent room.
   The patient must relax as much as possible and do not move and talk during the measurement procedure.
   The cuff should maintain at the same level as the right atrium of the heart.
   Do not cross your legs and keep your feet on the ground.
   Keep your back against the backrest of the chair.
   For a meaningful comparison, try to measure under similar conditions.
   For example, take daily measurements at approximately the same time, on the same wrist, or as directed by a physician.
   

Setting Up The Device

Firstly, make sure you set the time and data correctly so the device can register the results with the correct time.

1. With the monitor OFF, press and hold the SET button for 3 seconds. It will enter the SITTINGS Mode.
2. Press or hold the MEM button to adjust the Hour digits that are blinking on the display. Press SET to confirm.
3. Repeat step 2 for setting the Minutes; Month; Day and Year.
4. Once the Year is set, the display will show “mmHg” This is the standard measurement unit. Press SET to save. Or press MEM to change to “kPa” and then press SET to save.
5. Once the measurement unit is set, the LCD will show “DONE” and the device will shut off.

Preparing The Measurement

Before tying the cuff to your wrist, make sure you remove all accessories from the wrist (bracelets, watch, etc). Use the device on the wrist that doesn’t have poor circulation.

1. Roll up the sleeve to reveal the skin of the wrist.
2. Make sure to tie the cuff to 0.4 -o,6″ (1-1.5cm) from your wrist joints.
3. Tie the cuff to your wdst and keep the palm facing up.
4. Tie the cuff to your wrist tightly but not painfully.
5. Place your elbow on a table and make sure that the wrist is at the same level with your heart.
6. Rest 3 minutes; keep your palm upwards, back straight and breathe deeply for 5 or 6 times before starting the measurement

Taking A Measurement

1. After resting press the Start Button and the measuring procedure will start.
2. First the measured air pressure will calibrate to zero and then the device will inflate and start reading the blood pressure and heart rate.
3. When the measurement ls completed the results will appear In the screen. The measurement Is also saved In the memory.

Tips and Timing

• Sit with your back straight and supported.
• Your feet should be flat on the floor and not crossed.
• Before taking your blood pressure, empty your bladder and sit for 2 minutes while breathing early.
• Support your left arm on a flat surface and make sure the monitor is at heart level.
• For an accurate and clear result, please measure the left wrist every time. Blood circulation may differ from wrist to wrist so you can get a different result when you change wrists.
• Take off any jewelry around the left wrist or hand and do not measure over your clothes.
• Avoid hot drinks, caffeine, tobacco, food, alcohol and strenuous exercises at least 30 minutes before taking your blood pressure.
• Take your blood pressure at the same time every day and record the measurement In a notebook. Take multiple readings If necessary.
• Make sure you do not move or speak during a measurement
• Do not use the device in a cold environment.
• Do not shower or bathe 30 minutes prior to measuring.

Using the memory function

• Make sure that the date and time is set correctly.
• Every measurement is automatically saved in the memory, with a maximum capacity of 60 measurements;
• To view the recorded data press the MEM button while the monitor Is Inactive. If the monitor Is not yet Inactive, first deactivate It by pressing the start/stop button.
• Use the buttons MEM for Up and Set for Down to read through the records.

Deleting the records

In case you want to delete your recorded measurements, please follow these steps:

1. Make sure the monitor is inactive; press START/STOP if needed.
2. Press MEM to go to Memory.
3. Press and hold the MEM button for 3 seconds.
4. “DEL ALL” will start blinking. Press SET to confirm.
5. “DEL DONP will show, meaning the stored data Is deleted. The device will shut off.

Maintenance

1. Please make sure to place the device away from the sun.
2. Store it in a dry place.
3. When you want to clean the device, you should use a dry doth. Do not place it in water or clean it with wet cloths.
4. Also, be careful not to shake or throw the device.
5. For a better performance, keep it in a room with stable temperature and away from dust.
6. The cuff should not be cleaned as it may affect the accuracy of the reading.

Basic info about Blood Pressure

Systolic pressure means that the ventricles contract and pump out blood, increasing the blood pressure. The diastolic pressure means that the ventricles relax so the blood pressure decreases.

AHA Indicator

After each measurement an arrow indicates the corresponding category color on the left of the display. The colors represent the different categories of the American Heart Association blood pressure classification as depicted in the chart below.

High Blood Pressure
(hypertension) Stage 1| 130-139| or| 80-89
High Blood Pressure
(hypertension) Stage 2| 140 or higher| or| 90 or higher
Hypertensive Crisis
(Emergency care needed)| Higher than 180| and/or| Higher than 120

Changes in blood pressure

There are many factors that cause the blood pressure to change.
Weather, emotions, stress, food, physical activities; all these influence the variations in the blood pressure. Bear in mind that measuring in clinical settings tend to cause the blood pressure to increase. This is called “white coat effect”.

Error Messages and FAQ

with new batteries
Batteries are inserted incorrectly.| Insert the batteries correctly
Low batteries| Display is dim or display | Batteries are low.| Replace with new batteries
Error message| E 01 shows| The cuff is too tight or too loose.| Refasten the cuff and then measure again.
E 02 shows| The monitor detected motion, talking or the pulse is too poor while measuring.| Relax for a moment and then measure again.
E 03 shows| The measurement process does not detect the pulse signal.| Loosen the clothing on the wrist and then measure again.
E 04 shows| The treatment of the measurement failed.| Relax for a moment and then measure again.
EE XX, shows on the display.| A calibration error occurred.(XX can be some digital symbol, such as 01, 02,etc., if this similar situation appear, all belong to calibration error.)| Retake the measurement. contact the retailer or our If the problem persists, customer service department for further assistance. Refer to the warranty for contact information and return instructions.
“oUt ” shows| Out of measurement range.| Follow the instructions in user manual and measure again.
Power supply| 2 x AAA batteries B,3V
---|---
Display mode| Digital LCD V.A. 36 mmx 41 mm
Measurement mode| Oscillographic testing mode
Measurement range| Rated cuff pressure: 0mm Hg~299 mmHg (0 kPa ~ 39.9 kPa) Measurement pressure:
SYS: 60 mm Hg~230 mm Hg (8.0kPa~30.7 kPa) DIA: 40mmHg~130 mm Hg (5.3 kPa~17.3 kPa) Pulse value: (40-199)beat/minute
Accuracy| Pressure:
5 ºC-40 with in ± 3 mm Hg(0.4 kPa) Pulse value:±5%
Normal working condition| A temperature range of :+5°C to +40°C A relative humidity range of 15% to 90%, non-condensing, but not requiring a water vapour partial pressure greater than 50 hPa An atmospheric pressure range of : 700 hPa to 1060 hPa
Storage & transportation condition| Temperature:-20°C to +60°C
A relative humidity range of ≤ 93%, non condensing, at a water vapour pressure up to 50 hPa
Measurement perimeter of the wrist| About 13.5cm-21.5cm
Net Weight| Approx. 108g (Excluding the dry cells)
External dimensions| Approx. 80mm x 65mm x 22mm
Attachment Mode of operation| 2 x AAA batteries &, user manual
Continuous operation
Degree of protection| Type BF applied part
Protection against ingress of water| IP22: The first number 2: Protected against solid foreign objects of 12,5 mm and greater. The second number/ Protected against vertically falling water drops when enclosure titled up to 15º. Vertically falling drops shall have no harmful effects when the enclosure is titled at any angle up to 15º on either side of the vertical
|
Software version| A01
Device classification| Internally Powered ME Equipment

Important Symbols On The Monitor

| Symbol for “THE OPERATION GUIDE MUST BE READ”| | Symbol for “TYPE BF APPLIED PARTS”
---|---|---|---
| Symbol for “MANUFACTURE DATE”| | Symbol for “ENVIRONMENT PROTECTION – Electrical waste products should not be disposed of with household waste. Please recycle where facilities exist. Check with your local authority or retailer for recycling advice”
| Caution: These notes must be observed to prevent any damage to the device.
| Symbol for Serial Number| | This device has not been tested for use in an MR environment and should not be used exposed to MR environments while patients are wearing the device. Keep it outside the MPI scanner room.
| Symbol for “DIRECT CURRENT”
| Symbol for “RECYCLE”

EMC Guidance

The ME EQUIPMENT or ME SYSTEM is suitable for home healthcare environments.

Warning ：Don’t near active HF surgical equipment and the RF shielded room of an ME system for magnetic resonance imaging, where the intensity of EM disturbances is high.

Warning : Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper operation. If such use is necessary, this equipment and the other equipment should be observed to verify that they are operating normally.

Warning : Use of accessories, transducers and cables other than those specified or provided by the manufacturer of this equipment could result in increased electromagnetic emissions or decreased electromagnetic immunity of this equipment and result in improper operation.”

Warning : Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm (12 inches) to any part of the equipment , including cables species by the manufacturer. Otherwise, degradation of the performance of this equipment could result.

Technical description

1. All necessary instructions for maintaining BASIC SAFETY and ESSENTIAL PERFORMANCE with regard to electromagnetic disturbances for the excepted service life.

Guidance and manufacturer’s declaration -electromagnetic emissions and Immunity.

Manufacturer’s declaration on Electromagnetic Emissions for all ME Equipments and Systems

Guidance and manufacturer’s declaration – electromagnetic emissions

Emissions test| Compliance
RF emissions CISPR 11| Group 1
RF emissions
CISPR 11| Class B
Harmonic emissions IEC 61000-3-2| Not applicable
Voltage fluctuations/ flicker emissions
IEC 61000-3-3| Not applicable

Manufacturer’s declaration on Electromagnetic Immunity for all ME Equipment’s and Systems

Guidance and manufacturer’s declaration – electromagnetic Immunity

Immunity Test| IEC 60601-1-2 Test level| Compliance level
Electrostatic discharge (ESD) IEC 61000-4-2| ±8 kV contact
±2 kV, ±4 kV, ±8 kV,
±15 kV air| ±8 kV contact
±2 kV, ±4 kV, ±8 kV,
±15 kV air
Electrical fast transient/burst IEC 61000-4-4| Not applicable| Not applicable
Surge
IEC 61000-4-5| Not applicable| Not applicable
Voltage dips, short interruptions and voltage variations on power supply input lines
IEC 61000-4-11| Not applicable| Not applicable
Power frequency magnetic field
IEC 61000-4-8| 30 A/m
50Hz/60Hz| 30 A/m
50Hz/60Hz
Conducted RF IEC 61000-4-6| Not applicable| Not applicable
Radiated RF IEC 61000-4-3| 10 V/m
80 MHz – 2,7 GHz
80 % AM at 1 kHz| 10 V/m
80 MHz – 2,7 GHz
80 % AM at 1 kHz
NOTE UT is the a.c. mains voltage prior to application of the test level.

Manufacturer’s declaration on Electromagnetic Immunity for all ME Equipments and Systems that do not provide LIFE-SUPPORTING

Guidance and manufacturer’s declaration – electromagnetic Immunity

Radiated RF IEC 61000-4-3
(Test specifications for ENCLOSURE PORT IMMUNITY to
RF wireless communications equipment)| Test Frequency (MHz)| Band (MHz)| Service| Modulation| Maximum Power (W)| Distance (m)| Test Level (V/m)| Compliance level (V/m)
385| 380 –390| TETRA 400| Pulse modulation 18 Hz| 1,8| 0.3| 27| 27
450| 430 –470| GMRS 460,

FRS 460

| FM
± 5 kHz deviation 1 kHz sine| 2| 0.3| 28| 28
710| 704 –787| LTE Band 13,

17

| Pulse modulation 217 Hz| 0,2| 0.3| 9| 9
745
780
810| 800 –960| GSM 800/900, TETRA 800,
iDEN 820,
CDMA 850,
LTE Band 5| Pulse modulation 18 Hz| 2| 0.3| 28| 28
870
930
1720| 1700 – 1990| GSM 1800;
CDMA 1900;
GSM 1900; DECT;
LTE Band 1, 3, 4, 25; UMTS| Pulse modulation 217 Hz| 2| 0.3| 28| 28
1845
1970
2450| 2400 – 2570| Bluetooth, WLAN, 802.11 b/g/n,  RFID 2450,
LTE Band 7| Pulse modulation 217 Hz| 2| 0.3| 28| 28
5240| 5100 – 5800| WLAN 802.11 a/n| Pulse modulation 217 Hz| 0,2| 0.3| 9| 9
5500
5785

FCC Statement

This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) this device may not cause harmful Interference. and (2) this device must accept any Interference received, including Interference that may cause undesired operation.

Warranty

This Limited Warranty covers any defects in materials or workmanship under normal use during the Warranty Period. iProven will either replace the product or repair the product at no charge, using new or refurbished replacement parts. The Warranty Period of this iProven product is 2 years from the date of purchase. A replacement product or product part assumes the remaining warranty of the original product purchase. This Limited Warranty does not cover batteries and packaging, nor any problem that Is caused by conditions, malfunctions, or damage not resulting from defects in material or workmanship.

To obtain warranty service, contact 0ur customer support at www.iproven.com to determine the problem and the most appropriate solution far your situation.

iProven owns and reserves the rights comprised in the copyright of this document. No part of this document may be changed, copied, reproduced, or Imitated In any form or by any means without prior written consent of iProven. All statements, information, and recommendations in this document are provided “AS IS” without Warranties, guarantees or representations of any kind, either express or Implied. The information In this document is subject to change without notice. iProven reserves the right of final interpretation of this document.

Customer Support

DISTRIBUTED BY
NETDIRKT DISTRIBUTION, Ll.C
9360 Federal Blvd
Federal Heights, CO 80260, USA
Phone : 1-503·974-0913

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