4 EN
To avoid potential serious injury to the user and the patient and/or
damage to this device, the user must:
1. Read this operating manual thoroughly and be familiar with its
contents prior to using this equipment.
2. Carefully unpack the unit and check if any damage occurred
during shipment. If damage is detected, please refer to the
Service and Claims section in this manual.
3. Be a qualified physician, having complete knowledge of the use
of this equipment.
4. Test this equipment prior to a surgical procedure. This unit was
fully tested at the factory before shipment.
5. Attempt no internal repairs or adjustments not specifically
detailed in this operating manual.
6. Pay close attention to the care and cleaning instructions in this
manual. A deviation may cause damage.
7. Read the entire instruction manual before assembling or
connecting the unit.
The warranty is void if any of these warnings are disregarded.
Stryker Endoscopy accepts full responsibility for the effects on safety,
reliability, and performance of the equipment only if:
• Readjustments, modifications, and/or repairs are carried out
exclusively by Stryker Endoscopy.
• The electrical installation of the relevant operating room
complies with the applicable IEC, CEC, and NEC requirements.
Warning Federal law (United States of America) restricts this
device to use by, or on order of, a physician.
Stryker Endoscopy reserves the right to make improvements on the
product(s) described herein. Product(s), therefore, may not agree in detail
to the published design or specifications. All specifications are subject to
change without notice. Please contact the local Stryker Endoscopy
Distributor listed in the International Service section, or phone your local
Stryker Endoscopy sales representative or agent for information on
changes and new products.
Warnings and Cautions
