Riester ri-magic HPLED, Инструкция по эксплуатации

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If a reusable device shows signs of material deterioration, it should no longer be reused
and should be disposed of/claimed according to the procedures described in the Disposal/
Warranty sections
2.2. Accessories
Art. no.: 11340 Transformer 230 V/120 V
Art. no.: 11343 Stand with adapter, including base with 5 castors and tube
Art. no.: 11344 Adapter part between stand and lamp arm
Art. no.: 11345 Wall mount
Art. no.: 11346 Universal clamp
3. Technical specifications
Model: ri-magic®HPLED examination light
Table light/wall light/floor light
Input: 100 V - 240 V/50 - 60 Hz/0.6 A
Output: 5 V/3 A/15 W.
Light source: LED
Classification: type B
Working temperature: 0 °C to +40 °C, relative humidity between 30 and 75%
(non-condensing)
Storage place: -5 °C to +50 °C, up to 85% relative humidity (non-condensing)
Weight: table and wall model: approximately 2.5 kg
Floor model: approximately 7.5 kg
8. Maintenance
The instruments and their accessories require no special maintenance. If an instrument
needs to be tested for any reason, please contact Riester, or send it to an authorized Ries-
ter dealer in your area, the details of which we will provide you with upon request.
9. Standards
Photobiological safety of lamps and lamp systems DIN EN 62471 IEC 60601-1
10. Disposal of packaging
When disposing of the packaging material, pay attention to the appropriate waste regula-
tions. Keep out of reach of children.
11. Explosion hazard
Do not use this equipment in the presence of flammable anaesthetics, vapours or liquids.
12. Disposal of accessories and device
The service life of this ri-magic® HPLED is 10 years. At the end of its service life, the
ri-magic® HPLED, as well as its accessories, must be disposed of in compliance with the
guidelines regulating the disposal of such products. If you have questions regarding the
disposal of the product, please contact the manufacturer.
13. ELECTROMAGNETIC COMPATIBILITY ACCOMPANYING DOCUMENTS ACCORDING TO
IEC 60601-1-2, 2014, Ed. 4.0
During installation and operation of the device, observe the following instructions:
To avoid electromagnetic interference with the operation of the device, do not use the de-
vice at the same time as other electronic devices.
To avoid electromagnetic interference with the operation of the device, do not use or stack
the device near, on or under other electronic devices.
Do not use the device in the same room as other electronic devices, such as life-supporting
devices that have a significant impact on the life of the patient and treatment outcomes, or
other measuring instruments or treatment devices that use little electrical power.
Do not use cables or accessories that are not specified for the device, as this can increase
the emission of electromagnetic waves from the device and reduce the device‘s electroma-
gnetic immunity.
Caution:
Medical electrical equipment is subject to special precautions in terms of electromagnetic
compatibility (EMC).
Portable and mobile radio frequency communication devices can affect medical electrical
equipment. The ME device is intended for operation in a home health care electromagnetic
environment and for professional facilities such as industrial areas and hospitals.
The user of the device should ensure that it is operated within such an environment.
Warning:
The ME device may not be stacked, arranged or used directly next to or with other devices.
When use close to or stacked with other devices is required, the ME device and the other
ME devices must be monitored to ensure intended operation within this configuration. This
ME device is intended for use by medical professionals only. This device may cause radio
frequency interference or interfere with the operation of nearby devices. It may become
necessary to take appropriate corrective measures, such as redirecting or rearranging the
ME device or shield.
The ME device assessed does not exhibit any essential performance characteristics in the