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Chattanooga Intelect Transport 2 Manual Del Usuario página 43

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ELECTROMAGNETIC COMPATIBILITY (EMC) TABLES
AAMI STD ES 60601-1
CSA 22.2 NO. 601.1
IEC 60601-1
IEC 60601-1-6
NO. 60601-1-6
IEC 60601-2-5
NO. 60601-2-5
IEC 60601-2-10
NO. 60601-2-10
The Intelect® Transport 2 is intended for use in the electromagnetic environment specified below.
The customer or the user of the Intelect® Transport 2 should assure that it is used in such an environment.
Emissions test
RF emissions
CISPR 11
RF emissions
CISPR 11
Harmonic emissions
IEC 61000-3-2
Voltage fluctuations/
flicker emissions
IEC 61000-3-3
NOTE The EMISSIONS Characteristics Of this equipment make it Suitable for use in industrial areas and hospitals(CISPR 1 Class A).
If it is used in a residential environment (for Which CISPR I I Class B is normally required) this equipment might not offer adequate
protection to radio-frequency communication services. The user might need to take mitigation measures. such as relocating or re-
orienting the equipment.
Device conforms to the following standards:
Guidance and manufacturer's declaration – electromagnetic emissions
Compliance
Electromagnetic environment – guidance
The Intelect® Transport 2 uses RF energy only for its internal function. Therefore,
Group 1
its RF emissions are very low and are not likely to cause any interference in nearby
electronic equipment.
Class A
The Intelect Transport 2 is suitable for use in all establishments other than domestic,
and may be used in domestic establishments and those directly connected to the
public low-voltage power supply network that supplies buildings used for domestic
purposes, provided the following warning is heeded:
Class A
Warnig: This equipment/system is intended for use by healthcare professionals only.
This equipment/system may cause radio interference or may disrupt the operation
of nearby equipment. It may be necessary to take mitigation measures, such as re-
orienting or relocating the Intelect Transport 2 or shielding the location.
Complies
Medical electrical equipment Part 1:
General requirements for basic safety and essential performance
Medical electrical equipment – Part 1-6:
General requirements for basic safety and essential performance -
Collateral standard: Usability
Medical electrical equipment - Part 2-5:
Particular requirements for the basic safety and essential performance of
ultrasonic physiotherapy equipment
Medical electrical equipment - Part 2-10:
Particular requirements for the basic safety and essential performance of
nerve and muscle stimulators
APPENDIX
43

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