INTRODUCTION
This product is a
medical device.
Please make sure to read this manual before using.
This manual is to assure proper installation and usage.
Pay attention when reading the manual in order to properly use this product and to assure prolonged
lifespan of the product. Specifically, pay attention to the contents with marks such as , and .
<User>
•
Qualified Professional
<Intended use>
•This is a device that uses ultrasonic piezoelectric technology for surgery.
<Classification of equipment>
•
Type of protection against electric shock: Class I equipment
- To avoid the risk of electric shock, this equipment must be connected to the main electrical supply and
is properly grounded.
•
Degree of protection against electric shock: Type BF applied part
•
Classification according to the degree of protection against ingress of water as detailed in the current edition of IEC 60529:
- Control Box: IPX0
- Foot Controller: IPX8
•
Not suitable product to use where there exists flammable anesthetic mixture with air or with oxygen.
•
User sterile product (non-sterile product at shipment)
•
Classification according to mode of operation: Intermittent operation
•
Applied parts: Ultrasonic Tip
<Use time>
•
Loading time: 1 minutes
•
Resting time: 10 minutes
<Operation & Storage condition>
Operating condition
Transport and storage condition
Temperature (℃)
Relative humidity (%R.H.)
Atmospheric pressure (hPa)
Temperature (℃)
Relative humidity (%R.H.)
Atmospheric pressure (hPa)
10~35
10~80
700~1,060
-20~60
10~90
500~1,060
Type BF
2
Summary of Contents for PIEZOART
Page 1: ...USER MANUAL ...
Page 23: ...MEMO 22 ...
