Related Manuals for Verity Medical NeuroTrac MyoPlus Pro
Summary of Contents for Verity Medical NeuroTrac MyoPlus Pro
- Page 1 SERVICE MANUAL NeuroTrac MyoPlus Pro ® Verity Medical Ltd. Churchtown House, Tagoat, Co. Wexford, Ireland, Y35 XY44 Phone: +353 (0) 53 913 2433; +44 (0) 1794 367 110, support@veritymedical.com Doc.: MYO120P-SM-08, revised on 07/06/2024...
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Page 2: Table Of Contents
Contents Contents Page Warnings ................................3 Contraindications & Precautions ........................4 Description of MyoPlus Pro Unit & Functions....................6 Safety checks..............................8 Consumable Materials and Preventative Maintenance ................... 10 Cleaning Instructions ............................11 Troubleshooting .............................. 12 Technical Specification ........................... 13 Information regarding Electromagnetic compatibility and interference (EMC) .......... -
Page 3: Warnings
Warnings This unit must be used with the guidance of a Physiotherapist or Doctor. Type BF equipment, Continuous Operation. Do not insert lead wires into a mains power supply. Do not immerse unit into water or any other substance. The unit is not protected from the ingress of water droplets from a shower of rain if used outside the carrying case. -
Page 4: Contraindications & Precautions
Contraindications & Precautions Before using this equipment you must first seek the advice of your Physiotherapist or Doctor Read this operating manual before using this stimulator. Stimulator should not be used: By patients fitted with a demand style cardiac pacemakers unless so advised by their Doctor During pregnancy [unless medically advised] By patients with undiagnosed pain conditions By patients with undiagnosed skin, vaginal or rectal conditions... -
Page 6: Description Of Myoplus Pro Unit & Functions
Description of MyoPlus Pro Unit & Functions... -
Page 8: Safety Checks
This instruction defines the procedure to be followed and the criteria to be met in testing the NeuroTrac MyoPlus Pro of Verity Medical ltd. Only qualified and trained staff will carry out the Level 1 & 2 test. Test equipment Name Model &... - Page 9 Is the TFT display readable, can you read clearly the mA numbers when you use stimulation? Serial number of tested unit Pass/failed Fault description If the device is found to be faulty, please return it to the supplier for processing. Repairs can only be carried out by Verity Medical Ltd.
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Page 10: Consumable Materials And Preventative Maintenance
CONTROL UNIT Wipe the surface once a week with a damp cloth or antiseptic wipe. Do not use cleaning sprays or alcohol based cleaning solutions. Control unit disposal: please return to Verity Medical LTD or to the appointed distributor. ACCESSORIES... -
Page 11: Cleaning Instructions
Cleaning Instructions For single patient use, wipe the surface once a week with a damp cloth or antiseptic wipe. Always clean the unit before the use of another Patient. Remember: Probes and lead wires are for single patient use only! We recommend using Clinell Universal Wipes or WW1504 Patient Cleansing wet Wipes, suitable for hands and equipment wiping. -
Page 12: Troubleshooting
Troubleshooting If the programme cannot be changed - remove the battery cover and unlock the unit by pressing the unlock button. If mA intensity cuts out above 8 milliamps and zero mA is flashing on LCD: 1. The problem you are experiencing is most likely due to a poor connection of the two stainless steel electrode plates on the shaft of the probe in your body. -
Page 13: Technical Specification
Technical Specification Dual channel: individually isolated circuits. Amplitude: 0-90 mA into 500 Ohm load; indication only. Actual mA will tend to be less than indicated due to electrode impedance: at 1000 Ohms load (Electrodes in poor condition) the maximum will be limited to 86 mA, at 1500 Ohms load the maximum will be limited to 65 mA. Type: Constant Current, maximum output voltage 180 Volts +10 / -30 Volts Waveform: Symmetrical, rectangular bi-phasic with zero DC current. -
Page 14: Information Regarding Electromagnetic Compatibility And Interference (Emc)
Information regarding Electromagnetic compatibility and interference (EMC) NeuroTrac products are designed to produce very low levels of radio frequency (RF) emissions (interference), to be immune from effects of interference produced by other equipment operating in their vicinity and damage due to electrostatic discharge all when operating in a typical domestic and or clinical environment. -
Page 15: Electromagnetic Immunity
Table 202: Guidance and manufacturer’s declaration – Electromagnetic immunity The NeuroTrac ® product is intended for use in the electromagnetic environment specified below. The ® customer or the user of the NeuroTrac product should assure that it is used in such an environment, and that precautions regarding that environment are heeded. - Page 16 Table 204: Guidance and manufacturer’s declaration – Electromagnetic immunity The NeuroTrac® product is intended for use in the electromagnetic environment specified below. The customer or the user of the NeuroTrac® product should assure that it is used in such an environment. Immunity IEC 60601 Complian...
- Page 17 Table 206: Recommended separation distances between portable and mobile RF communications equipment and NeuroTrac® product The NeuroTrac® product is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the NeuroTrac® product can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the NeuroTrac®...
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Page 18: Warranty
Warranty Verity Medical Ltd., provides a warranty to the original purchaser, that this product will be free from defects in the material, components and workmanship, for a period of 2 years from the date of purchase by the distributor [invoice date from Verity Medical to the appointed distributor].
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