Instructions for use ENG

Instructions for use ENG
Instructions for use ENG
CLED11 PPS
Examination light
ENG
SYMBOLS
The warning symbols indicate all instructions that are important for safety. Failure to comply with them can lead to injury,
damage to the luminaire or the equipment. In combination with the following signal words the warning symbols means:
DANGER
Can lead to death or serious injury
WARNING
Can lead to injury
Comply with operating Instructions
CE conformity mark
Mainswitch: on
Mainswitch: off;
Appliance of protection class II
Storage humidity
Storage temperature
Disposal
Manufacturer
VARIANTS:
CLED11FX PPS
CLED11SX PPS
2
ENG
CONTENTS
1
SAFETY INSTRUCTIONS ........................................................................................................................................ 3
1.1
Intended use ................................................................................................................................................. 3
1.2
User profiles .................................................................................................................................................. 3
1.3
Safety instructions ......................................................................................................................................... 3
1.4
Warning levels ............................................................................................................................................... 4
2
SCOPE OF SUPPLY ................................................................................................................................................ 4
2.1
CLED11FX PPS ............................................................................................................................................ 4
2.2
CLED11SX PPS ............................................................................................................................................ 4
3
4
5
6
7
MOUNTING .............................................................................................................................................................. 4
OPERATION ............................................................................................................................................................ 4
DISINFECTION CLEANING ..................................................................................................................................... 4
SAFETY INSPECTIONS .......................................................................................................................................... 5
DEMOUNTING ......................................................................................................................................................... 5
7.1
Disposal ........................................................................................................................................................ 5
8
9
10
11
12
ACCESSORIES........................................................................................................................................................ 5
ADDITIONAL INSTRUCTIONS ................................................................................................................................ 5
TROUBLESHOOTING ............................................................................................................................................. 6
TECHNICAL DATA ................................................................................................................................................... 6
ELECTROMAGNETIC COMPATIBILITY (EMC) ...................................................................................................... 7
1
SAFETY INSTRUCTIONS
1.1
Intended use
The luminaire CLED11 is an examination luminaire. Its
intended use is to illuminate the body of the patient to
support diagnosis or treatment. An interruption of the
diagnosis or treatment caused by a light failure is always
possible without a risk for the patient. The luminaire can
not be used in operating rooms.




1.2
User profiles
Medical professional
A medical professional is any person who has completed
medical training and is working in his or her professional
field.
Cleaning professional
A cleaning professional is trained in national and jobrelated hygiene regulations.
Electrician
An electrician is trained in the fields of electronics and
electrical engineering and is familiar with the relevant
standards and regulations.
Qualified professional
A qualified professional is capable of mounting and
dismounting the luminaire thanks to professional training,
knowledge and experience and knowledge of the
regulations.
1.3



Safety instructions
Operation by a medical professional
The instructions form part of the product. They must
be stored and made accessible to all subsequent
users.
Any work on the luminaire (including repairs) must
be carried out by qualified electricians only.
Mounting must be performed by a qualified
professional only.











The luminaire must not be altered or manipulated in
any way. Only approved original parts must be used.
Any use other than the intended use with original
parts may give rise to other technical values and lifethreatening danger.
Operation in potentially explosive areas is prohibited.
The luminaire power supply is a potential ignition
source.
The luminaire must only be operated in dry, dust-free
rooms.
The luminaire must not be left switched on without
supervision.
Do not use any luminaire that is damaged. Defective
cables are also potential hazards. Do not place the
cable close to any heat source or on sharp edges.
Damage to the eyes. Never look directly into the light
source.
Replace any glass that is damaged before operating
the luminaire again.
Never place additional loads on the luminaire head
or the arm.
The luminaire must not be covered by a cloth or any
similar item while it is in operation.
The ventilation openings (where they exist) must be
free whenever the luminaire is in operation.
The luminaire must not be operated near to external
heat sources that exceed the maximum ambient
temperature of the luminaire.
The luminaire must not be used in environmental
conditions other than those for which it is intended.
The luminaire must only be used for the intended
use described in this document.
The manufacturer cannot be held responsible for any
injury or damage that is caused as a result of any
use other than the intended use or of any failure to
comply with safety instructions and warnings.
It’s recommended to protect the luminaire with an
additional earth leakage circuit breaker.
3
ENG
1.4
Warning levels
WARNING
DANGER
Indication of hazards that can lead to death or serious
injury if measures are disregarded.
Risk of eye damage
 Never look directly into the beam of light
WARNING
Indication of hazards that can lead to injury if
measures are disregarded.
CAUTION
Indication of hazards that can lead to damage to
property if measures are disregarded.
2
SCOPE OF SUPPLY
2.1
CLED11FX PPS


Insert power cable to the luminaire
Connect the power cable with the power supply

Switch the luminaire on/off
The following are included in the scope of supply:
5
DISINFECTION CLEANING
DANGER
Electric shocks are life-threatening
1x Luminaire
1x Power cable
2.2
CLED11SX PPS

Remove the connector from the power supply and
put the switch in the "OFF" position before the
disinfection celaning.
CAUTION
The following are included in the scope of supply:
Damage to property caused by incorrect cleaning




1x Luminaire
1x Power cable
3

4
MOUNTING
The luminaires are equipped with an adapter pin.
The luminaire must be positioned in one of the
accessories described in chapter 8.
OPERATION
DANGER
Electric shocks are life-threatening



4
Do not insert any power cable that is damaged.
If there is any sign of damage to the power cable,
replace it immediately with a new one.
The supply voltage and frequency must match the
data on the type plate.


No cleaning agents containing alcohol, solvents,
chlorine or abrasive products must be used. Those
agents can cause damages in the plastic parts.
The cleaning and disinfection agents must be
suitable and approved for plastics like PC, PMMA,
PA and ABS.
Concentrated disinfectants may damage the cover.
Pay attention to the specifications from the data
sheet of the agent for concentration and residence
time.
Unsuitable cloths can cause scratches.
NOTE
Dirt decreases luminosity


Clean regularly to keep the cover clean.
Disinfection only by wiping is permitted.
ENG
8

Clean the PMMA cover with a suitable cleaning cloth
and a suitable cleaning agent.
ACCESSORIES
Description
Item code
16mm MOBILE BASE
HWSCAM14255
COOLVIEW WALL
BRACKET ASSEMBLY
CABW14271
Rail Mount Bkt 16mm
CABKTR16
1 Meter Medirail kit.
Boxed with endcaps
CABKTRAIL
16mm Desk Clamp
OABKT16D
CAUTION
To minimize the risk of disease transmission, in
addition to complying with this user manual, you must
also comply with the applicable occupational health and
safety regulations and the requirements of national
bodies with responsibilities for hygiene and disinfection.
6
SAFETY INSPECTIONS
9
ADDITIONAL INSTRUCTIONS
The luminaire itself is maintenance-free.
You can obtain additional documents about this product
from the manufacturer upon request.
These luminaires do not affect any other devices.
To save energy, the luminaire should only be switched on
when actually needed.
DANGER
Electric shocks are life-threatening


Remove the connector from the power supply and
put the switch in the "OFF" position.
The connector cable must be checked for damage
at least once per year.
NOTE


7
Maintenance and repairs must only be carried out
by qualified electricians.
The corresponding user profile is described in
Chapter 1, Safety instructions
DEMOUNTING
DANGER
Electric shocks are life-threatening

7.1
Remove connector from the power supply and put
the switch in the "OFF" position before
demounting.
Disposal
Do not dispose the luminaire in household
refuse. Dispose the luminaire at a disposal
point in accordance with local regulations or
take them to a dealer that provides an
appropriate disposal service.
Cut off the cable directly on the housing.
The products listed above are more than
95% recyclable. The luminaires have been
constructed to be compatible with recycling
so that a high proportion of the materials
used in these products can be recycled or
converted into energy after the end of
service life. They contain no materials that
are dangerous or that need to be monitored.
5
ENG
10
TROUBLESHOOTING
Fault
Possible cause
Troubleshooting
User profiles
The luminaire does not light
Contact problem
Switch on again
All
The luminaire does not light
Lamp defective
Contact manufacturer
service
By manufacturer service only
The luminaire does not light
No mains voltage
Check mains voltage, check
all connections
Electrician
11
TECHNICAL DATA
Electrical:
Nominal input voltage
see type label of the luminaire
Frequency range
50/60Hz
Power consumption
13W (18VA)
Input current
0.09A
Power factor
0.72
Lighting data:
Central illuminance Ec at 1.0m (3.28 feet) distance
40‘000 lx *
Light field diameter d10 at 1.0m (3.28 feet) distance
Ø = 18cm (7.1“) *
Light field diameter d50 at 1.0m (3.28 feet) distance
Ø = 9cm (3.54“) *
Colour temperature
4400K *
Colour rendering index Ra
>93
Colour rendering index R9
>90
Total irradiance Ee at maximum intensity
<180 W/m
2
* -10% / +20% tolerance
Environmental conditions for transport, storage and operation:
Ambient temperature (storage and transport)
-20°C to +70°C (-4°F to +158°F)
Ambient temperature (operation)
+10°C to +35°C (+50°F to +95°F)
Relative humidity (non-condensing)
max. 75%
Weight:
CLED11FX PPS
1.4kg (3.09 lb)
CLED11SX PPS
1.4kg (3.09 lb)
Operating mode:
Operating mode
Continuous operation
Klassifizierung:
CLED11FX / SX PPS
Schutzklasse II
Degree of protection as per IEC 529
IP 20
According to standard 93/42/EWG
Class I
Electrical safety test and EMC according to:
EN/IEC 60601-1
EN/IEC 60601-2-41
EN/IEC 60601-1-2
GMDN-Code
12276
Service life of light source:
Service life LED
6
30‘000h (L70/B50)
ENG
12
ELECTROMAGNETIC COMPATIBILITY (EMC)
Electromagnetic emission guidelines
The medical device is intended for operation in an electromagnetic environment such as the one specified below. The user must
ensure that it is operated in such an environment.
Emissions
In accordance
Electromagnetic environment
High-frequency emissions
Group 1
The medical device uses HF energy exclusively for its internal function. This
(CISPR 11)
means that its HF emissions are very low, and it is unlikely that adjacent electronic
devices will receive interference.
High-frequency emissions
Class B
The medical device is intended for use in all facilities, including residential
(CISPR 11)
buildings and facilities that are directly connected (without a transformer) to the
same low voltage network as residential buildings.
Emissions from harmonics
Class A
(IEC 61000-3-2)
Emissions from voltage
Compliance
fluctuations/flicker (IEC 61000-3-3)
Electromagnetic interference resistance guidelines
The medical device is intended for operation in an electromagnetic environment such as the one specified below. The user must
ensure that it is operated in such an environment.
Interference resistance to
IEC 60601-1-2 testing
Conformity level of the
Electromagnetic environment
level
medical device
Electrostatic discharge (ESD) Contact discharge: ± 6 kV ± 6 kV
Floors made of timber, concrete or ceramics tiles
(IEC 61000-4-2)
Air discharge: ± 8 kV
± 8 kV
are preferred. Where synthetic floor covering is
used the relative humidity should be at least 30%.
Fast transients/
Power supply cables: ± 2
± 2 kV
The quality of the mains power supply should
electrical disturbance
kV
match that of a typical business or hospital
variables/
Longer input and
Not applicable
environment.
bursts (IEC 61000-4-4)
output cables: ± 1 kV
Surge voltages/surges
±1 kV phase-to-phase
±2 kV
The quality of the mains power supply should
(IEC 61000-4-5)
voltage
match that of a typical business or hospital
±2 kV phase-to-earth
±1 kV
environment.
voltage
Magnetic field in the power
3 A/m
3 A/m
In proximity of this medical device, do not operate
supply frequency (50/60 Hz)
devices with unusually strong network-frequency
(IEC 61000-4-8)
magnetic fields (transformer stations etc.) .
Voltage dips and short
Cut >95 %, 0.5 periods
Cut >95 %, 0.5 periods
The supply voltage quality should be that of a
interruptions
Cut 60 %, 5 periods
Cut 60 %, 5 periods
typical business or hospital environment. If the
to the power voltage
Cut 30 %, 25 periods
Cut 30 %, 25 periods
user requires continued function during any
(IEC 61000-4-11)
Cut >95 %, 5 seconds
Cut >95 %, 5 seconds
interruption of the energy supply system, we
recommend that the medical device be powered by
an uninterrupted power supply or a battery.
Radiated HF disturbance
3 V/m
3 V/m
Recommended minimum distance of portable and
variable (IEC 61000-4-3)
80 MHz - 2.5 GHz
mobile radio devices of PEIRP radiated power to
the medical device, including its cables: d = 1.17√P
Conducted HF disturbance
3 Vrms-value
3 Vrms-value
Recommended minimum distance of portable and
values (IEC 61000-4-6)
150 kHz - 80 MHz:
mobile radio devices of PEIRP radiated power to
the medical device, including its cables:
80MHz - 800MHz: d = 1.17√P
800MHz - 2.5GHz: d = 2.33√P
d = recommended safe distance [m], P = Rated Power of the sender [ W ]. Field strengths from fixed RF transmitters, as determined by an
electromagnetic site survey should be less than the compliance level in each frequency range.
Interference may occur in the vicinity of equipment marked with:
Recommended safe distances from portable and mobile HF communications equipment
Rated Power of the sender [ W ]
150 kHz - 800 MHz
800 MHz - 2.5 GHz
0.01
0.12 m (0.39 ft)
0.23 m (0.75 ft)
0.1
0.37 m (1.21 ft)
0.74 m (2.43 ft)
1
1.17 m (3.84 ft)
2.33 m (7.64 ft)
10
3.7 m (12.14 ft)
7.37 m (24.18 ft)
50
8.27 m (27.13 ft)
16.48 m (54.07 ft)
100
11.7 m (38.39 ft)
23.3 m (76.44 ft)
7
http://www.brandon-medical.com
e-mail: [email protected]
© Brandon Medical Co. Ltd. • D80.021.000 • 04.2014 • Index: 1.1 • Subject to modification • printed in Switzerland
These installation and operating instructions are for customer information only and will only be updated or replace upon request by the customer
Brandon Medical Co. Ltd.
Elmfield Road, Morley
Leeds
LS27 0EL
Telephone: +44 (0) 113 27 77393
Fax: +44 (0) 113 27 28844
Was this manual useful for you? yes no
Thank you for your participation!

* Your assessment is very important for improving the work of artificial intelligence, which forms the content of this project

Download PDF

advertisement