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Valleylab LigaSure - Type CF Equipment (IEC 60601-1);Defibrillator Proof; Liquid Spillage (IEC 60601-2-2, Clause 44.3); Static Electricity Discharge Interference (IEC 60601-1-2 and IEC 61000-4-2); Electromagnetic Interference

Valleylab LigaSure
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Standards and IEC Classifications
Technical Specifications
LigaSure Vessel Sealing Generator Service Manual 4-9
Type CF Equipment (IEC 60601-1)/Defibrillator Proof
This generator provides a high degree of protection against electric
shock, particularly regarding allowable leakage currents. It is type CF
isolated (floating) output and poses no fibrillation danger.
This generator complies with the ANSI/AAMI HF18 specifications
for “defibrillator proof” designation and IEC 60601-2-2.
Liquid Spillage (IEC 60601-2-2, clause 44.3)
This generator enclosure is constructed so that liquid spillage in normal use does
not wet electrical insulation or other components which, when wet, are likely to
affect adversely the safety of the generator.
Static Electricity Discharge Interference (IEC 60601-1-2
and IEC 61000-4-2)
This generator enclosure can withstand an 8 kV electrostatic air discharge.
Electromagnetic Interference
When placed on or beneath an activated Valleylab electrosurgical generator, this
generator operates without interference. The generator minimizes electromagnetic
interference to video equipment used in the operating room.
Electromagnetic Compatibility (IEC 60601-1-2 and
IEC 60601-2-2)
This generator complies with the appropriate IEC 60601-1-2 and 60601-2-2
specifications regarding electromagnetic compatibility.
Notice
The LigaSure should not be used adjacent to or stacked with equipment other
than specified in the LigaSure User Guide and Service Manual. If adjacent or
stacked use is necessary, the LigaSure should be observed to verify normal
operation in the configuration in which it will be used.
The LigaSure intentionally applies RF energy for diagnosis or treatment during
activation. Observe other electronic medical equipment in the vicinity during the
LigaSure activation for any possible adverse electromagnetic effects. Ensure
adequate separation of electronic medical equipment based on observed
reactions.
The use of accessories, other than specified in the LigaSure User Guide and
Service Manual, may result in increased emissions or decreased immunity of the
LigaSure.
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