Shortwave Diathermy Machine (Continuous and Pulsed)

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Description

GENERAL FEATURES

Product description Shortwave Diathermy Machine (Continuous and pulsed)
Clinical purpose To give relief to the patient from muscular skeletal pain and injuries, and pelvic inflammatory disease and commonly used in muscle relaxation, and to induce deep heating in tissue for therapeutic purposes.
Application Effective in Inflammation of shoulder joint, Elbow joint, Cervical spondylosis, chronic arthritis, Osteoarthritis, Ligament sprain in knee joints, Low back ache, muscle spasms, myositis, neuralgia, sprains and strains, tenosynovitis, tendonitis, bone injuries, bursitis, Sinusitis and wound healing etc.,
Technology Microprocessor controlled solid state
Types of diathermy applicator Induction field,Capacitive field
Touch Screen No
Type of display monitor LED
Screen saver facility after certain time selectable of inactivity Yes
Should have two outlets so that two electrodes can be used simultaneously with independent adjustment of peak power and pulse width Yes
Should have maximum of 100 free memory to save personal protocols Yes
Pulse frequency adjustable Yes
Special inductive electrode, inclusive Yes
Adjustable electrode arm Yes
HF cut-off switch in case of overload provided Yes
Patient safety swich provided Yes
Flexible pads: Metal electrodes encased in rubber and produce an electrostatic field Yes
Space plates: Consists of rigid metal electrode encased in a perplex cover of electrostatic field Yes
Coil or cable electrode consists of a wire with plug at either end creates electromagnetic field Yes
Mono mode: The flat rigid coil encased in plastic cover generates electromagnetic field Yes
The diplode or drum electrode consists of a flat coil electrode encased in a perspex cover with two wings generates electromagnetic field Yes
Safety instructions of usage lable pasted on the machine Yes
Do’s and Dont’s must be displayed on the machine with “Warning” instructions Yes
Additional precautions if any must be displayed on the machine lable Yes
The machine is mounted on castors with stoppers Yes
Size (HxWxL) (mmxmmxmm) 750x450x450
Weight (Kg) 31 to 50

OPERATIONAL & TECHNICAL REQUIREMENTS

RF Power source RF Generator solid state
RF Indicator Available
Input power supply 220+/-10% V, 50/60 Hz, AC Single phase
Power consumption (Watt) 250
Power output (Continuous mode)(Watt) 500 Watt
Power output (Pulsed mode) (Watt) 1000 Watt
Adjustable Output power settings 5 steps
Average power (Watt) 500 Watt
Peak power (Min) (Watt) 1000 Watt
Output frequency (MHz) 27.12
Wave length (mtr) 11.062
Wave shape Mono Phasic
Pulse rate or pulse repetition frequency in increments of 10 Hz, (Hz) 500 Hertz
Adjustable Pulse duration or Pulse width in increments of 20 micro seconds, (micro second) 400 microsecond
Treatment duration timer Manual & Pre-programmable
Treatment duration selectable Timer, manual (minute) 1 to 30
Treatment duration programmable digital timer (minute) 1 to 99
Pre-programmable settings to user protocols (Minimum) 20
Tuning control to adjust the radio frequency to maximum out put Yes
Automatic tuning of power between the electrodes and patient Yes
Testing tube filament to check the output of the machine provided Yes
Fuse 6 Amp Yes

STANDARD ACCESSORIES

Minimum Disc electrodes or space plates (No) 2
Minimum Rubber electrodes (Set) 2
Mono-polar inductive electrodes (No) 1
Diplode or drum electrodes (No) 1
Flat Coil electrodes (No) 2
High frequency cables (No) 2
Flexible cable to connect rubber electrode (No) 2
Felt spacers (No) 2

PACKING MODE

The product is packed individually in a wooden box including all the accessories in such a way that there will be no transit damage during transportation Yes

ENVIRONMENTAL CONSIDERATIONS

Storage conditions Temperature 0 deg C to 50 deg C, RH 10% to 90%
Work or usage environment Temperature 10 deg C to 50 deg C, RH 10% to 90%

CERTIFICATIONS & REPORTS

Submission of Test Report from Central Govt/NABL/ILAC accredited Lab to prove the conformity to declared specification at the time of supply YES
Should have safety certificate from a competent authority viz EU-CE/US-FDA/STQC/ERTL Yes
Certificate No CE – 3321
Certificate Date 15 MARCH 2018
Product certification EU-CE,US-FDA
Four digit number of notified body If product is EU-CE certified 3321
Product Certificate No 93 / 42 / EEC
Product Certificate Date 15 MARCH 2018
Certificate issuing authority UKISO.CO.UK
Certification, performance and safety standards specific to the device ISO 14971:2007
Submission of all the certifications and test reports to the buyer along with supplies on demand Yes

INSTALLATION & TRAINING

Supplier to perform on site installation, safety and operation checks before handover Yes
Training of users in operation and basic maintenance shall be provided Yes

WARRANTY & MAINTENANCE

On site Warranty (Year) 1
User technical and maintenance manual detailing complete maintaining schedule with routine maintenance should be provided Yes
Contact details of manufacturer, supplier and local service agent to be provided Yes

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