Leep Precision Patient Return Electrode - Cooper Surgical LEEP PRECISION LP-10-120 Manual De Funcionamiento

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U .S . Federal law restricts this device to sale by or on the order of a physician . This device
SHOULD NOT be used without proper training and preceptorship .
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For monopolar systems it is recommended to keep the voltage/power as low as possible to
achieve the desired end effect (due to the potential for capacitive coupling and inadvertent
burning at high voltages) .
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Adequate anesthesia is indicated for all electrosurgical procedures .
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Inspect loop and ball for adequate insulation .
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Avoid using an electric extension cord (danger of separation) .
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Use a Smoke Evacuator with this device .
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This device generates high-frequency energy that could, under some circumstances, cause
interference to other equipment .
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For situations where the MAXIMUM OUTPUT VOLTAGE is less than or equal to 1,600 V,
ASSOCIATED EQUIPMENT and ACTIVE ACCESSORIES should be selected that have a
RATED ACCESSORY VOLTAGE equal to or greater than the MAXIMUM OUTPUT VOLTAGE.
• ASSOCIATED EQUIPMENT and ACTIVE accessories should be selected with RATED
ACCESSORY VOLTAGE ≥ MAXIMUM OUTPUT VOLTAGE when the smaller of variable
y [see below] or the number 6 is ≤ CREST FACTOR for that HF SURGICAL MODE.
• When MAXIMUM OUTPUT VOLTAGE (Umax) is > 1,600 V, and the CREST FACTOR
is < the variable y calculated below, indicating that any ASSOCIATED EQUIPMENT and
ACTIVE ACCESSORIES used in such mode or setting must be rated to withstand the
combination of actual voltage and CREST FACTOR .
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No modification of this equipment is allowed.
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No customer-serviceable parts .
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Only replacement of power cords or fuses can be done by the user . Only replace with these
items with the exact replacement part(s) available from CooperSurgical .
Section 7 LEEP PRECISION Patient Return Electrode
A Patient Return Electrode must be used to operate the LEEP PRECISION Integrated System/Generator . The
Patient Return Electrode must be of the Split or Dual type for the safety features to prevent R/F burns due to
poor adhesion .
For optimum patient safety with the use of the LEEP PRECISION Integrated System/Generator,
it is strongly recommended to use ONLY authorized and genuine CooperSurgical LEEP
PRECISION Split/Dual Patient Return Electrodes . No other Patient Return Electrode has
been tested for use with this system .
Patient injury may result. Do not use a single/not split Patient Return Electrode as it is not
continuously monitored for integrity.
CAUTIONS
U – 400 [Volts]
max
y =
600 [Volts]
NOTE
WARNING
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