JOHARI DIGITAL Myolift QT, Инструкция по эксплуатации, Страница: 9 / 23

Myolift QT
Instruction Manual
8 | P a g e
DRAFT
8.2 TECHNICAL SPECIFICATIONS
Antenna Specification
•
Maximum Transmitted Power (dBm) - 0
•
Average Gain (dBi typ.) - -0.5
8.3 GUIDANCE AND MANUFACTURIN'S DECLARATION
ELECTROMAGNETIC COMPATIBILITY
Myolift QT complies with the requirements of IEC 60601-1-2:2014 (EMC Collateral standard) including the
E-field susceptibility requirements at a 3 V/m, at frequencies from 80 MHz to 2.7 GHz. However, even at
this level of device immunity, certain transmitting devices (cellular phones, two-way radios, cordless
phones, paging transmitters, RFID devices etc.) emit radio frequencies that could interrupt equipment
operation if operated in a range too close to the equipment. User should be aware of possible radio
frequency interference if hand held device is operated in close proximity to the equipment. Portable and
mobile RF communications equipment may affect the normal function of the Myolift QT.
Do not use cables or accessories other than those provided with the Myolift QT system, as this may result
in increased electromagnetic emissions or decreased immunity to such emissions.
If the
Myolift QT system is used adjacent to or stacked with other equipment, observe and verify normal
operation of the system in the configuration in which it will be used prior to using it
.
Hand held and mobile RF communications equipment may a ff ect the normal function of the
Myolift QT.
Do not use cables or accessories other than those provided with the Myolift QT system, as this
may result in increased electromagnetic emissions or decreased immunity to such emissions.
If the Myolift QT system is used adjacent to or stacked with other equipment, observe and
verify normal operation of the system in the configuration in which it will be used prior to using
it.
Test Electrical Safety environment – guidance
IEC 60601-1:2005+AMD1:2012
Medical Electrical Equipment Safety standards,
IEC 60601-2-10:2012+AMD1:2016 Part 2: Particular requirements for the safety of nerve and muscle
stimulators
IEC 60601-1-11:2015 Part 1-11: General requirements for basic safety and essential
performance
— Collateral standard: Requirements for medical
electrical equipment and medical electrical systems used in the
home healthcare environment
Guidance and manufacturing's declaration – electromagnetic emissions
Mode Waveform Level /Intensity Pulse Width Frequency Output (Vpp)
Educate Symmetrical
Biphasic Sq.
Wave
Level 1 (Low) 60 m sec 0.9 Hz; 0.08 V
Level 2 (High) 60 m sec 0.694 Hz; 0.155 V
Erase Level 1 (Low) 400 m sec 0.625 Hz 0.08 V
Level 2 (High) 400 m sec 0.625 Hz 0.155 V