Technical data
Mains power:
Power consumption:
Fuse sets:
Life time of the lamp:
Minimum distance from light source to
patient:
Working distance from light source
to patient:
Central illuminance E c :
Light field diameter d
(at a 30 cm
10
working distance):
Overall irradiance:
Colour temperature:
Colour rendering index R a :
Special colour index R 9 :
Environmental conditions for operation:
Temperature:
Relative humidity:
Air pressure:
Environmental conditions for storage
and transport:
Temperature:
Relative humidity:
Air pressure:
Protection class:
Operation altitude:
Protection provided by enclosures
(IP code):
Risk group (according to DIN EN 62471) 1 (low risk)
Weight incl. wall mount:
Weight of clamp mount:
Length of flexible arm:
*
smallest light field and at a 30 cm working distance, depending on t
Emission test
RF emissions CISPR11
RF emissions CISPR 11
Harmonic Emissions
IEC 61000-3-2
Voltage Fluctuations/Flicker
Emissions IEC 61000-3-3
12/64
100– 240 V AC, 50/60 Hz
33 VA
2 x T 2A H 250 V
approx. 30,000 hours
20 cm
30 cm
*
≥ 45,000 lx
approx. 8.5 – 14 cm
Typically 115 W/m
2
≥ 3000 K
≥ 85
Typically 58
+10 °C to +35 °C
10 % to 75 %
700 hPa to 1060 hPa
-20 °C to +50 °C
10 % to 95 %
500 hPa to 1060 hPa
I
3000 m
IP20
approx. 2.6 kg
approx. 0.2 kg
97 cm
Guidance and manufacturer's declaration – electromagnetic emissions
The EUT is intended for use in the electromagnetic environment specified below.
The customer or the user of the EUT should assure that it is used in such environment.
Compliance
Group 1
EUT uses RF energy only for its internal function. Therefore, RF-emission is very low and it is
unlikely that any interference in nearby electronic equipment.
Class B
The EUT is suitable for use in all establishments, including domestic establishments and those
directly connected to the public low-voltage power supply network that supplies buildings used for
domestic purposes.
Warning: This device is intended only for use by medical professionals. This is a device of class A
CISPR 11 in the domestic environment, this device may cause radio interference, so that it may be
necessary in this case, to take appropriate remedial measures, as e.g. orientation, new arrange-
ment or shielding of the MEG or restrict the connection to the site.
Class A
Symmetrical three-phase EUTs and other EUTs.
Passed
med 0413
General instructions
Condensation can form when moving from a cold to a warm environment.
Wait until the unit has warmed up and is absolutely dry before using it.
Proper functioning is only guaranteed if original spare parts and
accessories from HEINE are used.
The expected life cycle amounts with designated use and the observation
of warning and safety information as well as the maintenance instructions
up to 7 years. Beyond this period, the product may continue to be used if
it is in a safe and good condition.
Electromagnetic Compatibility
Medical electric devices are subject to special precautionary measures with
regard to electromagnetic compatibility (EMC). Portable and mobile high
frequency communication equipment can affect medical electric devices.
This device is intended for use by medical professionals in the electro-
magnetic environment specified below. The user of this device should
assure that it is used in such an environment
The use of accessories, converters or cables other than the ones
specified by HEINE might lead to increased emission reduced electrical
immunity of the medical equipment.
The ME device may not be stacked directly near or used directly beside
other devices. If the ME device is to be operated in a stack or with other
devices, the device should be watched to ensure it operates properly in
this location.
Electromagnetic environment – Guidelines
2018-03-15