Anspach eG1 Manual De Instrucciones página 8

English
• Use of accessories or cables other than those provided by DePuy Synthes Power Tools and specified for use with
eG1 System may result in increased emissions or decreased immunity.
• The eG1should not be used adjacent to or stacked with other equipment and that if adjacent or stacked use is
necessary, the eG1 should be observed to verify normal operation in the configuration in which it will be used. Do
not stack equipment which is heavier than 13.6 kg (30 lbs ).
• Medical Electrical Equipment needs special precautions regarding EMC and needs to be installed and put into
service according to the EMC information provided in this accompanying documentation.
• Portable and Mobile RF communications equipment can affect Medical Electrical Equipment.
• Power source should comply with applicable IEC, CEC, and NEC requirements. Grounding reliability can only be
achieved when this equipment is connected to a receptacle marked "HOSPITAL GRADE."
• Do not use in oxygen rich environment.
• No modification of this equipment is allowed.
• Do not modify. Modifications could result in loss of electrical safety.
• Dispose of items contaminated with body fluids with other biohazardous waste.
• At end of life recycle or dispose of device in accordance with local and national regulations.
• To avoid the risk of electric shock, this equipment must only be connected to a supply main with protective earth.
The use of Accessories, transducers, and cables other than those specified, with the exception of transducers
and cables sold by the Manufacturer of this device as replacement parts for internal components, may result in
increased Emissions or decreased Immunity of the eG1 System.
Cautions
• United States Federal law restricts this device to sale by or on order of a physician or other licensed healthcare
provider.
• Do not use accessories other than those provided by DePuy Synthes Power Tools and specified for use with
Anspach Systems.
• To insure equipment operates as designed, read and follow manufacturer's instructions.
• Do not operate handpiece without an attachment and the corresponding dissection tool.
• Only Anspach G1 Dissection Tools should be used with G1 Systems.
• Use care to protect hose when handling, cleaning, and during system use.
• Damage to hose can cause leaking, rupture, or other related failures.
• Do not step on, set equipment on, pinch, kink, clamp, or otherwise occlude handpiece hose during use.
Latex Information
Not made with natural rubber latex.
Warranty & Return Policies
Warranty and return policy is available upon request.
Warning: All Instrument System components returned for servicing or repair should be properly cleaned and sterilized
as applicable prior to shipping.
Warning: Transmissible Spongiform Encephalopathies (TSE)
DePuy Synthes Power Tools will not authorize or accept the return of products that directly contact patients or
are contaminated with a patient's body fluids who is suspected or confirmed with a Transmissible Spongiform
Encephalopathies/ Creutzfeldt-Jakob Disease (TSE/CJD) diagnosis. DePuy Synthes Power Tools recommends that
all Anspach products used on a patient confirmed with a TSE/CJD diagnosis be incinerated. Anspach Dissection Tools
used on a patient suspected of TSE/CJD diagnosis must be incinerated.
Contact your Sales Representative for replacement of product incinerated under this policy or for temporary equipment
while original equipment is quarantined. Contact the DePuy Synthes Power Tools Customer Service Department
regarding TSE/CJD contamination for additional information.
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