Kurabo QuickGene-Auto240L, Руководство по эксплуатации

Страница: 7 / 78

v
QuickGene-Auto240L Operation Manual
Laser Standards
The laser sensor used in this system for detecting the workpiece/consumables is classified as "Class 1"
according to standard IEC60825-1 in accordance with stipulation in FDA Laser Notice No. 50.
The barcode reader (light source component) for reading the barcode on blood sample collection tubes
is classified as “Exempt Group” in accordance with standard IEC62471.
The 2-dimensional barcode reader (target pointer component for reading position adjustment) for
reading the code on collection tubes is classified as "Class 1" in standard IEC60825-1 in accordance
with stipulation in FDA Laser Notice No. 50.
NB: The 2-dimensional barcode reader is an optional component for this system. It is implemented
only when included as an option.
Do not attempt to peer into the system and directly view the barcode reader or
2-dimensional code reader red light source during the sample ID reading operation.
Direct viewing at length may cause eye disorders.
Operation with a procedure other than indicated in the operation manual may lead
to exposure to dangerous laser irradiation.
Laser Device Specification
Specification/Name
Laser Sensor
(for detection of workpiece/consumables)
2-Dimensional Code Reader
(for reading collection tube information)
Wavelength (nm) 655 660
Output (mW) 0.39 0.06
Coverage Angle (º)
X direction: 0.20
Y direction: 0.53
－
Laser Class
CLASS 1 Laser Product
(IEC60825-1
：
2007
FDA (CDRH) Part 1040.10)
CLASS 1 Laser Product
(IEC60825-1
：
2007
FDA (CDRH) Part 1040.10)
Ultraviolet Light (UV) Irradiating Function
Operation of the UV irradiating function of this system will cause a small quantity
of ultraviolet leakage from the sliding door window, fan area, joints with exteriors,
etc. Exposure to ultraviolet light may cause damage such as eye or skin irritation.
Avoid exposure of skin or eyes to ultraviolet light.
Warning:
Warning:
Warning: