2
5.To protect the users eyes and avoid risk of thermal injury during an endoscopic examination, use only the minimum amount
of brightness required.
6. During clinical procedures, avoid unnecessary prolonged use which could compromise patient/user safety.
7. Continually monitor this equipment and the patient for any signs of irregularities.
8. In the event that some type of irregularity is noted to the patient or this equipment, take the appropriate action to ensure
patient safety.
9. If the operation of any of the components of the endoscopic system fails during the procedure and the visualization of the
procedure is lost or compromised, place the endoscope in the neutral position and slowly withdraw the endoscope.
10. This equipment should only be used according to the instruction and operating conditions described in this manual. Failure
to do so could result in compromised safety, equipment malfunction or instrument damage.
1-5. AFTER USE
1. Refer to the operating instructions supplied with all the components of the endoscopic system to establish the right order in
which components should be turned OFF. Some peripheral devices may have to be turned OFF first to avoid compromising
their operation.
2. Wipe all surfaces clean with gauze slightly dampened with alcohol.
3. Be sure connector interfaces and ventilation ports are not allowed to become wet or splashed with liquids.
1-6. STORAGE
1. This equipment should NEVER be stored in areas where the unit could get wet or be exposed to any environmental
conditions such as high temperature, humidity, direct sunlight, dust, salt, etc., which could adversely affect the equipment.
2. This equipment should NEVER be stored in the presence of flammable or explosive gases or chemicals.
3. This equipment should NEVER be stored or transported in an inclined position, nor should it be subjected to impact or
vibration.
4. Cords, accessories, etc., should be cleaned and neatly stored.
5. This equipment should be maintained in a clean condition during storage and be ready for subsequent use.
1-7. SERVICE
1. Alterations/modifications to the equipment should NEVER be made. Repairs should only be performed by an authorized
PENTAX service facility.
2. When replacing the lamp, use only the lamp recommended by PENTAX and follow all PENTAX instructions provided.
1-8. MAINTENANCE
Periodically this equipment and any applicable accessories should be inspected for operation and safety.
1-9. DISPOSAL
The equipment should be returned for disposal to PENTAX. Contact your local PENTAX representative or service facility.
1-10. FOR THE STATE OF CALIFORNIA, USA ONLY
Perchlorate Material-special handling may apply. See www.dtsc.ca.gov/hazardouswaste/perchlorate.
Perchlorate Material: Lithium battery contains perchlorate.
An information on Disposal for users in the European Union
This product is a medical device. In accordance with European Directive 2002/96/EC on Waste Electrical and Electronic
Equipment, this symbol indicates that the product must not be disposed off as unsorted waste, but should be collected
separately. Contact your local PENTAX distributor for correct disposal and recycling.
By disposing of this product correctly you will help ensure that the waste undergoes the necessary treatment, recovery
and recycling and thus prevent potential negative effects on the environment and human health which could otherwise
arise due to inappropriate waste handling.
Summary of Contents for EPK-1000
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