The document summarizes the instructions and specifications for a tens unit device. It provides details on controls and features, directions for use in different modes, user parameters that can be adjusted, electrode placement and skin care, battery information, safety information including indications, contraindications and warnings. It also lists the accessories included, warranty period and physical specifications of the device.
This document provides instructions and specifications for a TENS (transcutaneous electrical nerve stimulation) unit. It includes information on controls and features, directions for use, user parameters for different modes, electrodes and skin care instructions, and safety information. The different modes include normal, burst, modulated, and strength duration. For each mode, it describes the default and adjustable settings for parameters like frequency, pulse width, and treatment time. It also provides contact information for customer service and technical support.
The document is a user manual for the TruWave tens unit. It provides instructions on how to operate the device, including turning it on and off, adjusting settings like intensity levels, treatment times and modes. It describes the different stimulation modes the device offers and how to program parameters within each mode. The manual also contains information on skin preparation, electrode usage, battery replacement, indications for use, contraindications and safety precautions. Specifications for the device like dimensions, accessories included and warranty information are also listed.
Hướng dẫn sử dụng máy đo bức xạ và cường độ sóng vô tuyến RF Tenmars TM-93Tenmars Việt Nam
Hướng dẫn sử dụng máy đo bức xạ và cường độ sóng vô tuyến RF Tenmars TM-93
https://tenmars.vn/san-pham/may-do-buc-xa-tenmars-tm-93/
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This document provides instructions for use of the In TENSity 5000 TENS Stimulator. It includes information on parts of the device, general safety warnings, instructions for use including how to turn the device on and off and adjust settings, specifications, cleaning and care instructions, troubleshooting tips, and other use details. The manual describes how the device uses transcutaneous electrical nerve stimulation (TENS) to help reduce various types of pain by sending electrical pulses to nerves under the skin that reduce the body's perception of pain signals.
This document provides supplemental instructions for using the NeuroMove system to treat stroke and spinal cord injury patients in a hospital clinic setting. It outlines a 10-step process for clinicians: 1) assessing patients, 2) creating a treatment plan, 3) using muscle stimulation, 4) starting in manual mode, 5) progressing to automatic mode, 6) adjusting stimulation parameters, 7) treating additional muscle groups, 8) monitoring patient compliance, 9) incorporating mCIMT therapy, and 10) using multi-channel EMG to improve muscle coordination. The goal is to efficiently develop patients' muscle function and motor skills to maximize recovery.
This document provides instructions and specifications for a TENS (transcutaneous electrical nerve stimulation) unit. It includes information on controls and features, directions for use, user parameters for different modes, electrodes and skin care instructions, and safety information. The different modes include normal, burst, modulated, and strength duration. For each mode, it describes the default and adjustable settings for parameters like frequency, pulse width, and treatment time. It also provides contact information for customer service and technical support.
The document is a user manual for the TruWave tens unit. It provides instructions on how to operate the device, including turning it on and off, adjusting settings like intensity levels, treatment times and modes. It describes the different stimulation modes the device offers and how to program parameters within each mode. The manual also contains information on skin preparation, electrode usage, battery replacement, indications for use, contraindications and safety precautions. Specifications for the device like dimensions, accessories included and warranty information are also listed.
Hướng dẫn sử dụng máy đo bức xạ và cường độ sóng vô tuyến RF Tenmars TM-93Tenmars Việt Nam
Hướng dẫn sử dụng máy đo bức xạ và cường độ sóng vô tuyến RF Tenmars TM-93
https://tenmars.vn/san-pham/may-do-buc-xa-tenmars-tm-93/
https://tenmars.vn/danh-muc/do-buc-xa-dien-tu-truong/
This document provides instructions for use of the In TENSity 5000 TENS Stimulator. It includes information on parts of the device, general safety warnings, instructions for use including how to turn the device on and off and adjust settings, specifications, cleaning and care instructions, troubleshooting tips, and other use details. The manual describes how the device uses transcutaneous electrical nerve stimulation (TENS) to help reduce various types of pain by sending electrical pulses to nerves under the skin that reduce the body's perception of pain signals.
This document provides supplemental instructions for using the NeuroMove system to treat stroke and spinal cord injury patients in a hospital clinic setting. It outlines a 10-step process for clinicians: 1) assessing patients, 2) creating a treatment plan, 3) using muscle stimulation, 4) starting in manual mode, 5) progressing to automatic mode, 6) adjusting stimulation parameters, 7) treating additional muscle groups, 8) monitoring patient compliance, 9) incorporating mCIMT therapy, and 10) using multi-channel EMG to improve muscle coordination. The goal is to efficiently develop patients' muscle function and motor skills to maximize recovery.
The document provides an overview of modernist art in the early 20th century. It discusses the development of styles like Fauvism, German Expressionism, Cubism, Dada, and Surrealism. Key events discussed include the influence of World War I, the Armory Show of 1913 which introduced modern European art to American audiences, and post-war Expressionist works by German artists like Beckmann and Dix addressing the trauma of the war. The document uses over 50 figures to illustrate important works in these styles by artists such as Matisse, Kandinsky, Picasso, Duchamp, and others.
This document provides an overview of art from the modern to postmodern eras in the later 20th century. It discusses how World War 2 shifted the center of western art from Paris to New York. Modernist styles like abstract expressionism, minimalism, and conceptual art are examined. The document also explores postmodern reactions like pop art, earthworks, and new organic architectures. Key artists and their representative works from each movement are illustrated to understand the theories and styles and critique of modernism in late 20th century art.
This document provides an overview of 16th century art in Northern Europe and Spain during the Protestant Reformation. It discusses key events like the rise of Protestantism led by Martin Luther and the resulting Catholic Counter-Reformation. Important artists from this period like Durer, Cranach, Holbein and others are mentioned along with their works that explored religious and political ideas through imagery. Architecture from this time in countries like France, Germany and the Netherlands is also summarized.
This document provides a user manual for the IF8100 interferential therapy device. It includes sections on device controls, electrode placement, skin care, batteries, customer service information, and treatment protocols for pain relief, edema reduction, spasm reduction and other indications. Treatment protocols provide recommendations on electrode placement, intensity levels, treatment times, recommended modes and stimulation parameters.
The IF8100 is an interferential therapy device with multiple treatment modes for pain relief and muscle stimulation. Key information from the document includes:
- Interferential therapy uses two channels of 4000Hz stimulation in a cross-pattern to penetrate the skin more effectively than TENS or NMES devices. The beating frequency can be set from 1-150Hz.
- Treatment modes include Low (1-10Hz), High (80-150Hz), Muscle (6s on/6s off at 50Hz), and Combo (cycles through other modes).
- Electrodes are placed in a cross-pattern around the treatment area. Intensity is set as high as comfortably tolerated. Typical treatment is 20
The document provides an overview of modernist art in the early 20th century. It discusses the development of styles like Fauvism, German Expressionism, Cubism, Dada, and Surrealism. Key events discussed include the influence of World War I, the Armory Show of 1913 which introduced modern European art to American audiences, and post-war Expressionist works by German artists like Beckmann and Dix addressing the trauma of the war. The document uses over 50 figures to illustrate important works in these styles by artists such as Matisse, Kandinsky, Picasso, Duchamp, and others.
This document provides an overview of art from the modern to postmodern eras in the later 20th century. It discusses how World War 2 shifted the center of western art from Paris to New York. Modernist styles like abstract expressionism, minimalism, and conceptual art are examined. The document also explores postmodern reactions like pop art, earthworks, and new organic architectures. Key artists and their representative works from each movement are illustrated to understand the theories and styles and critique of modernism in late 20th century art.
This document provides an overview of 16th century art in Northern Europe and Spain during the Protestant Reformation. It discusses key events like the rise of Protestantism led by Martin Luther and the resulting Catholic Counter-Reformation. Important artists from this period like Durer, Cranach, Holbein and others are mentioned along with their works that explored religious and political ideas through imagery. Architecture from this time in countries like France, Germany and the Netherlands is also summarized.
This document provides a user manual for the IF8100 interferential therapy device. It includes sections on device controls, electrode placement, skin care, batteries, customer service information, and treatment protocols for pain relief, edema reduction, spasm reduction and other indications. Treatment protocols provide recommendations on electrode placement, intensity levels, treatment times, recommended modes and stimulation parameters.
The IF8100 is an interferential therapy device with multiple treatment modes for pain relief and muscle stimulation. Key information from the document includes:
- Interferential therapy uses two channels of 4000Hz stimulation in a cross-pattern to penetrate the skin more effectively than TENS or NMES devices. The beating frequency can be set from 1-150Hz.
- Treatment modes include Low (1-10Hz), High (80-150Hz), Muscle (6s on/6s off at 50Hz), and Combo (cycles through other modes).
- Electrodes are placed in a cross-pattern around the treatment area. Intensity is set as high as comfortably tolerated. Typical treatment is 20
This document provides a user manual for the IF8100 interferential therapy device. It includes sections on device controls, electrode placement, treatment protocols, and technical specifications. The manual describes how to use the device for applications such as pain relief, edema reduction, and muscle spasm reduction. It provides guidance on treatment parameters and recommended modes for different therapeutic goals.
The document provides a user manual for an interferential therapy device called the IF8100. It includes instructions on device controls, recommended electrode placement and protocols for various applications including pain relief, edema reduction, spasm reduction and increasing local blood circulation. Protocols are provided for different treatment modes and include details on frequency settings, intensity levels and treatment duration. The manual also covers device start-up, supplies ordering information, technical specifications and safety information.
This document provides instructions and specifications for a muscle stimulation device. It begins with instructions for setup and use, including how to turn the device on/off, adjust stimulation levels, and set various treatment parameters like frequency, pulse width, and timing. It then provides safety information, listing appropriate uses as well as contraindications. Technical specifications are provided at the end, including output details and device dimensions. Contact information is also included for customer support.
This document provides instructions and specifications for a muscle stimulation device. It begins with instructions for setup and use, including how to turn the device on/off, adjust stimulation levels, and set various treatment parameters like frequency, pulse width, and timing. It then provides safety information, listing appropriate uses as well as contraindications. Technical specifications are provided at the end, including output details and device dimensions. Contact information is also included for customer support.
This document provides instructions and specifications for a muscle stimulation device. It begins with instructions for setup and use, including how to turn the device on/off, adjust stimulation levels, and set various treatment parameters like frequency, pulse width, and timing. It then provides safety information, listing appropriate uses as well as contraindications. Technical specifications are provided at the end, including output details and device dimensions. Contact information is also included for customer support.
This document provides instructions and specifications for a muscle stimulation device called the E-Wave. It outlines how to operate the controls and set parameters like stimulation level, frequency, pulse width, and treatment time. Safety information is also included, listing indications for use to treat muscle conditions, as well as contraindications like not using it on the carotid sinus nerves or transcerebrally. Warnings, precautions, electrode use, battery replacement, and technical specifications are also summarized.
This document provides instructions and specifications for a muscle stimulation device. It contains information on how to operate the device, including setting stimulation levels, frequencies, pulse widths, treatment times, and other parameters. Safety precautions are also outlined, such as not placing electrodes over the carotid sinus or transcerebrally. Technical specifications for the device include an output range of 0-100 mA, frequencies from 4-100 Hz, pulse widths from 50-300 microseconds, and dimensions of 2.5 x 5.5 x 1.0 inches.
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This instruction manual provides directions for using a TENS device. It includes sections on device parts, safety warnings, use instructions, specifications, cleaning and care, troubleshooting, and warranty information. The directions explain how to apply electrodes to the skin, turn the device on/off, select modes and intensities, and care for the device and electrodes. The specifications section provides technical details on waveforms, channels, battery, and timer. Troubleshooting addresses issues like weak stimulation, discomfort, and intermittent output.
This instruction manual provides directions for using a TENS device. It includes sections on device parts, safety warnings, use instructions, specifications, cleaning and care, troubleshooting, and warranty information. The directions explain how to apply electrodes to the skin, turn the device on/off, select modes and intensities, and care for the device and electrodes. The specifications section provides technical details on the device's channels, battery, pulse rates, waveforms, and programs.
This instruction manual provides directions for using a TENS device. It describes the device parts, general safety warnings, instructions for use including how to apply electrodes and adjust settings, cleaning instructions, troubleshooting tips, and other important information. The device has two channels, uses a 9V battery, and offers various therapy modes that can be adjusted including pulse width, rate, and intensity. Electrodes are placed on the skin to deliver electrical pulses to treat pain.
This instruction manual provides directions for using a TENS device. It describes the device parts, general safety warnings, instructions for use including how to apply electrodes and adjust settings, specifications, cleaning instructions, and troubleshooting tips. The device has two channels that can be used individually or together to stimulate different areas. It offers various therapy modes that adjust pulse width and rate, including normal, burst, and modulation modes. Electrodes are placed on the skin in areas indicated by a physician and connected to the device to provide pain relief therapy.
This instruction manual provides directions for using a TENS device. It includes sections on device parts, safety warnings, use instructions, specifications, cleaning and care, troubleshooting, and warranty information. The use instructions describe how to apply electrodes to the skin, turn the device on/off, select modes and settings, and adjust intensity levels. The device has two channels, adjustable pulse width and rate, and timer and modulation modes for pain relief therapy. Electrodes and lead wires should be cleaned or replaced regularly to ensure optimal and safe stimulation.
This instruction manual provides directions for using a TENS device. It includes sections on device parts, safety warnings, use instructions, specifications, cleaning and care, troubleshooting, and warranty information. The directions explain how to apply electrodes to the skin, turn the device on/off, select modes and intensities, and care for the device and electrodes. The specifications section provides technical details on the device's channels, battery, pulse rates, waveforms, and programs.
This document provides instructions for using pressotherapy lymphatic drainage equipment. It describes pressotherapy as a 30-minute pneumatic massage treatment using an inflatable boot that improves lymphatic drainage, fluid retention, and cellulite. The manual then details the equipment features, including 9 massage modes and adjustable pressure and timing. It concludes with technical specifications, operation instructions, and a packing list.
The Pressure Right wrist strip measures 5.5 inches long by 1 inch wide and has a hard plastic button 1.5 inches from the end that is 0.52 inches in diameter and 0.27 inches high. It is made of low-density perforated polyethylene film with an acrylate adhesive and the plastic button is made of medical-grade acrylonitrile butadiene styrene plastic through an injection molding process.
The Pressure Right wrist strip is designed to apply targeted pressure to the P6 acupressure point on the wrist to help reduce nausea and vomiting. It uses an adhesive backing to keep the plastic dome firmly placed over the P6 point for an extended period, providing relief without medication. The strip is applied using a locator guide to identify the P6 point on both wrists. Placing the plastic dome over the marked points and securing the adhesive strip helps stimulate the P6 point within five minutes to alleviate nausea and vomiting associated with conditions like surgery, chemotherapy, or motion sickness.
The NEUROMOVE is a neurological rehabilitation tool that has been proven to help patients recover lost movement from strokes and other conditions. It works by training healthy neurons to assume the functions of damaged brain cells through a concept called neuroplasticity. The device can be used even without muscle movement and is suitable both for clinical use and for patients to use at home for 30 minutes a day over 4-5 months to provide dramatic recovery results.
Zmpczm0170001003 ZMPCZM017000.10.03 Neuromove clinical presentation from Pain...Painezee Specialist
The NeuroMove is an EMG-triggered neuromuscular relearning device that uses electrical stimulation to reinforce attempted movements in patients with stroke, traumatic brain injury, spinal cord injury, and other neurological conditions. It detects muscle activity through electrodes and provides electrical stimulation as a reward when activity surpasses a threshold, helping to retrain motor control through neuroplasticity. Clinical studies have found the NeuroMove effective in regaining function for chronic stroke patients by improving proprioceptive feedback through activity time-locked to movement attempts.
ZMPCZM017000.10.03 Neuromove clinical presentation from PainEzeePainezee Specialist
The NeuroMove is an EMG-triggered neuromuscular relearning device that uses electrical stimulation to reinforce attempted movements in patients with stroke, traumatic brain injury, spinal cord injury, and other neurological conditions. It detects muscle activity through electrodes and provides electrical stimulation as a reward when activity crosses a threshold, helping to retrain motor control pathways in the brain. Clinical studies have found the NeuroMove effective in regaining function for chronic stroke patients by improving proprioceptive feedback through intensive, repetitive therapy sessions using this brain retraining tool.
ZMPCZM017000.10.03 Neuromove clinical presentation from PainEzeePainezee Specialist
The NeuroMove is an EMG-triggered neuromuscular relearning device that uses electrical stimulation to reinforce attempted movements in patients with stroke, traumatic brain injury, spinal cord injury, and other neurological conditions. It detects muscle activity through electrodes and provides electrical stimulation as a reward when activity crosses a threshold, helping to retrain motor control pathways in the brain. Clinical studies have found the NeuroMove effective in regaining function for chronic stroke patients by improving proprioceptive feedback through intensive, repetitive therapy sessions using this brain retraining tool.
The document summarizes the features and benefits of the MY TENS device, which is designed for home use transcutaneous electrical nerve stimulation (TENS) therapy. Key points:
- MY TENS is certified for safety and designed for easy home use without complicated settings. It provides a preset operating program to effectively treat most pain conditions.
- The device has an ergonomic design that allows for simple, flexible application to any part of the body. It also ensures the electrical signal is transmitted intact from the device to the patient.
- MY TENS can be discreetly used in public as it can be placed under clothes. It is also affordable and reusable through replacement of consumable parts.
This document declares that the NexWave Combo Muscle Stimulator and similar products manufactured for other distributors meet the essential health and safety requirements of the European Community. The manufacturer, Zynex Medical, Inc., used conformity assessment procedures and standards including ISO 13485 for quality management, IEC 60601 for electrical safety of medical equipment, and EN 1041 for information supplied by manufacturers. Thomas Sandgaard, President and CEO of Zynex Medical, Inc., signed the declaration on November 18, 2011.
This document provides instructions for electrode placement for various neuromuscular electrical stimulation (NMES) treatments. It describes the patient positioning and placement of the red and black electrodes on the body for treatments targeting the biceps, triceps, elbow flexion, elbow extension, wrist and finger flexion, shoulder abduction, and ankle dorsiflexion. Electrode placement may require trial and error to find the correct spots using low level stimulation. Additional targeted muscle groups and placements are described in the user manual.
Zywie Medical Devices Private Limited has commenced a collaboration with the Medical Devices Division of Juno Pharm from October 13, 2013. This collaboration will help both companies capture their full potential and help expand their business footprint in pain management medical devices across India. Ms. Chavali Anilaja announced the collaboration.
The document discusses the benefits of exercise for mental health. Regular physical activity can help reduce anxiety and depression and improve mood and cognitive function. Exercise causes chemical changes in the brain that may help protect against developing mental illness and improve symptoms for those who already suffer from conditions like anxiety and depression.
This document provides instructions for connecting electrodes for a TENS (transcutaneous electrical nerve stimulation) unit. It notes that the unit has two lead wires that should be connected to opposite electrodes in a diagonal configuration as shown in the diagram, and that the lead wire colors do not matter as long as the connections are diagonal.
This document provides instructions for proper electrode placement for a TENS (transcutaneous electrical nerve stimulation) unit. It notes that the unit has two lead wires that should be connected to opposite electrodes in a diagonal configuration as shown in the included diagram. The document also specifies that the lead wire colors do not matter and can be placed on either the top or bottom of the area being treated.
1. This document provides instructions for using NeuroGraph software to conduct biofeedback sessions. It describes how to select a patient, choose a protocol, attach sensors, monitor signals in real-time, set goals and provide feedback.
2. The user's guide explains how to review session data, including graph displays, replay functions, and report generation. Customization options allow modifying graph types, colors, and other display settings.
3. Advanced features include creating schedules with multiple trials, setting trial properties, and exporting data. The guide provides details on protocol customization, system settings, and other administrative functions for configuring and managing NeuroGraph software.
This document provides a user's guide for NeuroGames software. It describes how to install and set up the software, select protocols, create and edit protocols, manage patients, run protocols, view reports and save session data. Key steps include checking the instrument settings, selecting or creating a protocol, selecting a patient, running the protocol, and viewing saved session reports. The guide also describes options for password protection, confidentiality settings, and alternative protocol types including jungle and star light games.
The document provides an overview and instructions for using the IncontiMed Checklist software. It describes how to select a patient, administer a checklist to collect patient responses, generate reports on completed checklists, and manage patient records and settings. The software is designed to collect self-reported information from patients on incontinence experiences and supports customization of report templates, password protection, and displaying initials instead of names for patient confidentiality.
The document provides an overview and instructions for using the Headache Checklist software. It describes how to select a patient, administer the checklist questions, generate reports, and manage patient records and settings. The software allows clinicians to collect self-reported headache information from patients and create standardized reports in a HIPAA-compliant manner. It can be used as an assessment tool alongside a clinical evaluation to help evaluate headache complaints.
This document provides instructions for using ChiroScan software to conduct electromyography (EMG) scans. It describes connecting hardware, installing and registering the software, configuring instruments and protocols, and conducting scanning procedures. The scanning procedure involves preparing the skin, applying sensors coated with electrode gel to specific sites on the back, and collecting EMG data to measure muscle activity levels. The software analyzes the data and can generate reports comparing results to normative values.
This document contains information about dermatome charts, peripheral nerve charts, and motor point locations for electrostimulation therapy. The dermatome charts show the cutaneous nerve innervation patterns for the front, back, and foot. The peripheral nerve charts display the branches of the cervical, brachial, lumbar, and sacral plexuses. The motor point sections provide diagrams of the anterior and posterior muscle motor points for the trunk, upper extremities, and lower extremities.
There are two types of nerve fibers that transmit signals from the body to the brain. Large nerve fibers called nociceptive fibers do not transmit pain signals, while small nerve fibers do transmit pain signals. A TENS unit works by using electrical currents to stimulate the large nerve fibers, which prevents the small pain fibers from reaching the brain. This stimulation of large fibers closes the "gate" in the spinal cord to pain signals from the small fibers, providing pain relief. This mechanism is known as the "gate control theory of pain."
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Cell Therapy Expansion and Challenges in Autoimmune DiseaseHealth Advances
There is increasing confidence that cell therapies will soon play a role in the treatment of autoimmune disorders, but the extent of this impact remains to be seen. Early readouts on autologous CAR-Ts in lupus are encouraging, but manufacturing and cost limitations are likely to restrict access to highly refractory patients. Allogeneic CAR-Ts have the potential to broaden access to earlier lines of treatment due to their inherent cost benefits, however they will need to demonstrate comparable or improved efficacy to established modalities.
In addition to infrastructure and capacity constraints, CAR-Ts face a very different risk-benefit dynamic in autoimmune compared to oncology, highlighting the need for tolerable therapies with low adverse event risk. CAR-NK and Treg-based therapies are also being developed in certain autoimmune disorders and may demonstrate favorable safety profiles. Several novel non-cell therapies such as bispecific antibodies, nanobodies, and RNAi drugs, may also offer future alternative competitive solutions with variable value propositions.
Widespread adoption of cell therapies will not only require strong efficacy and safety data, but also adapted pricing and access strategies. At oncology-based price points, CAR-Ts are unlikely to achieve broad market access in autoimmune disorders, with eligible patient populations that are potentially orders of magnitude greater than the number of currently addressable cancer patients. Developers have made strides towards reducing cell therapy COGS while improving manufacturing efficiency, but payors will inevitably restrict access until more sustainable pricing is achieved.
Despite these headwinds, industry leaders and investors remain confident that cell therapies are poised to address significant unmet need in patients suffering from autoimmune disorders. However, the extent of this impact on the treatment landscape remains to be seen, as the industry rapidly approaches an inflection point.
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Integrating Ayurveda into Parkinson’s Management: A Holistic ApproachAyurveda ForAll
Explore the benefits of combining Ayurveda with conventional Parkinson's treatments. Learn how a holistic approach can manage symptoms, enhance well-being, and balance body energies. Discover the steps to safely integrate Ayurvedic practices into your Parkinson’s care plan, including expert guidance on diet, herbal remedies, and lifestyle modifications.
Osteoporosis - Definition , Evaluation and Management .pdfJim Jacob Roy
Osteoporosis is an increasing cause of morbidity among the elderly.
In this document , a brief outline of osteoporosis is given , including the risk factors of osteoporosis fractures , the indications for testing bone mineral density and the management of osteoporosis
Our backs are like superheroes, holding us up and helping us move around. But sometimes, even superheroes can get hurt. That’s where slip discs come in.
Muktapishti is a traditional Ayurvedic preparation made from Shoditha Mukta (Purified Pearl), is believed to help regulate thyroid function and reduce symptoms of hyperthyroidism due to its cooling and balancing properties. Clinical evidence on its efficacy remains limited, necessitating further research to validate its therapeutic benefits.
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2. Page 2
Table of Contents:
Customer Service / Supplies / Support
Pg
3
Get Started with the TruWave
Pg
4
Controls and Features
Pg
4
Directions for Use
Pg
5
Factory Settings
Pg
6
User Parameters
Pg
7
Electrodes and Skin Care
Pg 10
Batteries
Pg 11
Indications
Pg 11
Contraindications
Pg 11
Safety
Pg 11
Precautions
Pg 12
Warnings
Pg 12
Specifications
Pg 13
Caution:
Federal Law restricts this device to sale by or on the order of a practitioner licensed by the law of the State in which he/she practices to use or
order the use of the device.
3. Page 3
Zynex Medical
Painezee
Contact Information
0091-9030022402
(866) 940-7030
CUSTOMER SERVICE
Supplies:
To order more electrodes or other accessories
Technical Support:
Questions or problems with using your device
Device Return:
Order a postage paid return envelope to return your
device at no charge
(800) 495-6670
0091-9030022402
MAIN OFFICE
Billing Questions:
Questions regarding insurance benefits and
covered benefits for durable medical equipment or
questions about an Explanation of Benefits form
you received in the mail
FAX NUMBER
(800) 495-6695
MAILING ADDRESS
Zynex Medical
Plot No: 6, Green Avenues,
9990 Park Meadows Drive Nizampet Road,
Opp:Bhavyas Anandham,
Lone Tree, CO 80124ad - 500090
Kukatpally, Hydera
b
Andhra Pradesh, India
EMAIL
info@painezee.com
WEBSITE
zynexmed.com
www.painezee.com
info@zynexmed.com
4. Page 4
Get Started with the TruWave
Make sure the electrodes are placed properly on the skin (see “Electrodes and
skin care” for details) and that the lead wires are properly connected.
Turn on the unit by pressing ON for more than 1 second. The right LED will
illuminate, indicating that the leads and electrodes are properly connected and
that the unit functions properly.
Keep pressing ↑ on either channel until a comfortable level is reached, as
indicated by your physician or therapist.
To stop treatment, keep pressing ↓ on the channel used until display and light
goes out after 1 additional second (mA will go to zero first). Thereafter remove the electrodes and place them on the plastic pad.
Stimulation will run continuously until the treatment timer is changed or the
unit is turned off.
Controls and features.
The arrows on each side of the device will control only the intensity, unless
the Program button is pressed and the display will indicate which parameter is
being programmed.
These same arrows on the right side also serve as On or Off buttons. To turn
the device On, press the Arrow-button marked “On” for more than one second. To turn off the device, press the Arrow-button marked Off for more than
three seconds and it will turn off.
Programming is done as described below by pressing the middle button,
“Program”, which is used to scroll through a number of options.
5. Page 5
Directions for Use.
Turn unit ON and OFF: Press ON for 1 second to turn the unit on. The display will light up and the right LED will illuminate. Keep pressing OFF to
turn the unit off. It takes one additional second after reaching 0 mA to turn it
off. If no controls have been touched for five minutes with level at 0 mA or
five minutes after timeout, the TruWave will automatically turn off.
Setting Stimulation Level: Use ↑ and ↓ controls to increase or decrease level.
Do not use the PRG button. After 20 seconds the stimulation level is electronically locked as a safety feature to prevent the patient from unintentional
increase in stimulation. To increase, just press ↓ to reduce it by at least 1 mA,
which will unlock the safety feature. Thereafter you have 20 seconds to increase to desired level, before the lock is activated again. Any change in level
or mode will unlock the level.
Setting Mode: Press PRG once and use ↑ or ↓ to scroll between Normal,
Burst, Modulated and Strength Duration (SD) Modes.
Setting the Treatment Time: Press PRG four times and use ↑ or ↓ to select
the desired Treatment Time. Keep pressing ↑ to set a Continuous Treatment
Time.
Setting Frequency: Press PRG twice and use ↑ or ↓ to increase or decrease
the frequency of the Normal, Burst or Modulated modes. In SD mode the frequency is always fixed at 100 Hz, so this is not programmable.
SettingPulse Width: Press PRG three times and use ↑ or ↓ to increase or decrease the pulse width in Normal, Burst, or Modulated modes. In SD mode
the pulse width is fixed at 225 µsec.
Compliance data: Press PRG five times and use ↓ to display the usage time
in minutes and number of times used, when prompted by text in display. Only
stimulation levels above 5 mA are recorded as usage time. The compliance
meter can be reset by pressing ↑ to show prompt in display and thereafter
press ↓ twice to reset both parameters to zero.
6. Page 6
Return to factory settings: Press PRG six times and display will
prompt the choice to reset all parameters to factory settings. This is
particularly useful if the user is unsure if the settings are correct and is
a good starting point for variations.
Factory settings are:
Normal
Frequency
Pulse Width
Burst
Modulated
70 Hz
2 Hz
66-100 Hz
100 Hz
200 µsec.
200 µsec.
200 µsec.
200 µsec.
50%
Span
6 sec.
Cycle Time
Treatment Timer
Strength Duration
60 min
60 min
6 sec.
60 min
60 min
7. Page 7
User Parameters:
Normal Mode:
The default frequency is 70Hz, but as described in the section “Directions
for Use” can be set with intervals of 5Hz between 21Hz and 160 Hz and with
intervals of 1Hz between 2 and 20 Hz. The stimulation frequency is an indication of how often each stimulation pulse occurs, i.e. 70Hz means 70 stimulation pulses per second.
The default Pulse Width is 300 µsec, but as described in the section
“Directions for Use” can be set with intervals of 5µsec. between 50 and 400
µsec. The stimulation Pulse Width is an indication of how long the stimulation lasts during each stimulation pulse, i.e an indication of the “strength” of
the stimulation. An increase of Pulse Width will therefore be felt similar to
an increase in intensity.
The treatment timer is set default to 20 minutes, but as described in the section “Directions for Use” can be set with intervals of 10 minutes between
Continuous and up to 90 minutes. The treatment timer will count down as
shown in the display and stimulation will drop to zero after time is out. The
user can commence a new treatment session by increasing the level as desired.
The User can program the following parameters: Frequency, Pulse Width
and Treatment Time.
8. Page 8
Burst Mode:
The default frequency is 2 Hz, but as described in the section “Directions for
Use” can be set with intervals of 0.5 Hz between 0.5 Hz and 4 Hz. The Burst
Frequency is an indication of how often each train of pulses (eight pulses)
occurs. Each of the eight pulses in the pulse train consists of 50-400µsec
wide pulses each 10 millisecond (100 Hz). Burst stimulation is best applied
when the intensity is set to a level where visible, yet comfortable contractions at the rate of the burst frequency are present. The effect is usually felt
after 15 minutes or more of burst stimulation.
The treatment timer is set default to 20 minutes, but as described in the section “Directions for Use” can be set with intervals of 10 minutes between
Continuous, 10 minutes and up to 90 minutes. The treatment timer will count
down as shown in the display and stimulation will drop to zero after time is
out. The user can commence a new treatment session by increasing the level
as desired.
The User can program the following parameters: Burst Frequency, Pulse
Width and Treatment Time.
Modulated Mode:
The frequency will shift (modulate) between 66 and 100 Hz with a preset
interval of 6 seconds between each end frequency. The Pulse Width will also
shift (modulate) during the 6 seconds interval from 50µsec. to 400 µsec.
around the set Pulse Width. The Cycle Rate can be programmed between 5
and 12 seconds, but is preset at 6 seconds at default. The default Pulse Width
is 225µsec. and when the frequency is at it’s minimum, the Pulse Width is at
it’s maximum and visa versa.
The treatment timer is set default to 20 minutes, but as described in the section “Directions for Use” can be set with intervals of 10 minutes between
Continuous and up to 90 minutes. The treatment timer will count down as
shown in the display and stimulation will drop to zero after time is out. The
user can commence a new treatment session by increasing the level as desired.
The User can program the following parameters: Pulse Width, Cycle Rate
and Treatment Time.
9. Page 9
SD Mode:
Strength Duration (SD). The Frequency is fixed at 100Hz in this mode.
The Pulse Width as well as the intensity will vary in opposite ways
during an interval of 6 seconds. The Span is preset to 50%, so the pulse
width decreases to 50% of the set pulse width and up to 50% above.
Simultaneously, the Intensity increases to 50% of the set value and
decreases to 50% above. The pulse width is set at 225µsec. and can not
be changed. The energy delivered through the electrodes therefore remains constant, due to the increase of the intensity while the pulse
width decreases and visa versa.
The treatment timer is set default to 20 minutes, but as described in the
section “Directions for Use” can be set with intervals of 10 minutes
between Continuous and up to 90 minutes. The treatment timer will
count down as shown in the display and stimulation will drop to zero
after time is out. The user can commence a new treatment session by
increasing the level as desired.
The User can program the following parameters: Span, Cycle Rate and
Treatment Timer.
10. Page 10
Electrodes and Skin Care
The TruWave comes with 4 self-adhesive electrodes, 2” x 2” square.
These electrodes are for multiple use, pre-wired and fit directly into the
lead wires. The lead wires attach to the connectors at the top of the device,
while the other end of the lead wires, consisting of two pins, will attach
directly to the electrodes. For each channel used there must always be two
electrodes connected and placed on the skin to complete the circuit for the
electrical current to flow.
Proper skin care will help make the use of this device more comfortable
and trouble-free. Prior to treatment, wash the areas where the electrodes
will be placed with mild soap and water, rinse and dry the skin thoroughly.
If necessary, remove excess body hair.
The TruWave is intended to be used with re-usable, self-adhesive electrodes. Extended number of uses can be obtained by adding water to the
adhesive surface immediately after each use and placing them on the plastic pad. They will regain their conductivity and adhesiveness as compared
to leaving them dry.
Sterile electrodes may be required for some post-op applications.
11. Page 11
Batteries
One 9 volt Alkaline battery is used. The battery compartment on the
back of the device opens by sliding the cover downwards. Please
ensure to dispose the used batteries properly.
Rechargeable batteries are not recommended as they only have a short
usage time and are not charged while in the device.
The display will indicate “Batt Low” when the voltage of the batteries
drops below the level for satisfactory function. A red flashing LED will
also lead the attention to replacing the battery. Please replace the
battery with a new Alkaline battery in this event.
The TruWave accommodates a 9 Volt battery even if it is
inserted with reverse polarity and the TruWave circuitry will
ensure full functionality with reverse polarity.
Indications, contraindications, precautions, safety and warnings.
Safety References
Zynex Medical (Zynex) is only responsible for the safety, reliability and
function of the device when repairs, adjustments and changes have been
carried out by persons authorized by Zynex for such work and the device is
used according to the user manual. Repairs and technical safety tests shall only
be carried out by trained personnel.
Indications
This Zynex device has been designed for pain relief and should only be used
under supervision for adjunctive therapy for the treatment of medical diseases
and conditions.
Contraindications
•
The device must not be used on patients with cardiac pacemaker.
•
The stimulation must not be applied transcerebrally.
•
The device must not be applied with undiagnosed pain syndromes until
etiology is established.
•
Electrodes should not be placed so that current will be applied to the
•
carotid sinus (neck) region or transcerebrally (through the head).
12. Page 12
Warnings
•
This device is not effective for pain of central origin (This includes headache).
•
The safety of tens devices for use during pregnancy or birth has not been established.
•
This device should only be used under the continued supervision of a physician.
•
This device does not have curative value.
•
This device offers symptomatic treatment and as such suppresses the sensation
of pain which would otherwise serve as a protective mechanism.
•
The user must keep the device out of reach of children.
•
Electronic monitoring equipment (such as ECG monitors and ECG alarms)
may not operate properly when this device is in use.
Stimulation should not be applied transthoracically in that the introduction of electrical current into the heart may cause cardiac arrhythmias.
Precautions
•
Some patients may experience skin irritation or hypersensitivity due to the
electrical stimulation or electrical conductive medium. The irritation can usually be
reduced by using an alternate conductive medium, or alternate electrode placement.
•
If the stimulation levels are uncomfortable or become uncomfortable, reduce
the stimulation amplitude to a comfortable level and contact your physician if problems persist.
Effectiveness is highly dependent upon patient selection by a person qualified in the
management of pain patients.
Adverse Reactions:
Skin irritation and burns beneath the electrodes are potential adverse reactions.
13. Page 13
Specifications.
Dimensions:
Weight:
Accessories:
Warranty:
Left channel
Output
Programming
2.5 x 5.5 x 1.0 in.
8 oz. incl. Battery.
2 lead wires, one 9 Volt battery,
carrying case, users manual and
one pack of electrodes.
3 Years
6 months manufacturers warranty on
materials and workmanship.
Accessories excluded.
Right channel
Output
Readout Display
Indicator LED’S
Left channel Up
and Down
Right channel Up
and Down