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SYSMEX CyFlow Ploidy Analyser - General Safety; Laser Radiation Hazards; Electrical Hazards; Alterations to the Device

SYSMEX CyFlow Ploidy Analyser
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3 Safety
16
CyFlow™ Ploidy Analyser | Operating Manual | October 2021
3.8 General safety
The system operates with the reagents stated in the scope of operation,
such as Hypochlorite Solution and Decontamination Solution. For further
information please see chapter 4.3 Scope of delivery.
The waste bottle collects all used substances, its contents are not able to
re-enter the fluidic system by design.
Important information regarding the safe handling, transport and disposal
of reagents is contained in the related Safety Data Sheets.
Always meet the national and international guidelines and regulatory
standards for PPE (personal protective equipment).
Find Safety Data Sheets for our products at www.sysmex-partec.com.
3.9 Laser radiation hazards
The device is equipped with a class IIIb laser unit. If the housing of the
device is closed, the laser class of the laser unit is classified as a laser
class I (EN 60825-1).
The device complices with 21 CFR 1040.10 and 1040.11 except for
deviations pursuant to Laser Notice No. 50, dated June 24, 2007.
Only authorised service personnel is allowed to open the housing of the
device.
Laser light of laser class IIIb can be emitted if the housing of the device is
damaged or the laser protection is removed. Serious injuries of the eyes
and the skin could results from emission by laser light of class IIIb lasers.
3.10 Electrical hazards
The main electrical source used must be grounded or earthed due to local
specifications. The mains cable carries out the protective earthing. Please
place the device in such a way that the electrical power cord can easily be
unplugged. Removable power cords should be replaced by adequate
power cords only.
Beware of possible voltage when changing the fuse (T 3.15 A 250 V).
3.11 Alterations to the device
Unauthorised alterations to the device can result in risks and hazards. Therefore, unless
expressly permitted by the manufacturer, no alterations may be made to the device.
If the device is altered, appropriate tests and trials must be performed to ensure the
continued safe use of the device.

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