Barco AMM215WTTP, Руководство пользователя

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R5911667 /03 AMM215WTTP 32
Recommended Separation Distances Between Portable and Mobile RF
Communications Equipment and the AMM215WTTP system
The AMM215WTTP system is intended for use in an electromagnetic environment in which radiated RF
disturbances are controlled. The user of the AMM215WTTP system can help prevent electromagnetic
interference by maintaining a minimum distance between portable and mobile RF communications equipment
(transmitters) and the AMM215WTTP system as recommended below, according to the maximum output
power of the communications equipment.
Rated maximum output
power (W) of transmitter
Separation distance (m) according to frequency of transmitter
150 kHz to 80 MHz
d=1.17,
√ P
80 MHz to 800 MHz
d=1.17,
√ P
800 MHz to 2.5 GHz
d=1.17,
√ P
0.01 0.12 0.12 0.23
0.1 0.37 0.37 0.74
1 1.17 1.17 2.33
10 3.70 3.70 7.37
100 11.70 11.70 23.30
For transmitters rated at a maximum output power not listed above, the recommended separation distance (d)
in meters (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is
the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.
At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and
reflection from structures, objects, and people.
7.6 Explanation of symbols
Overview
You may find the following symbols (nonrestrictive list):
Indicates the device meets the requirements of the applicable EC directives/
regulations.
Indicates compliance with Part 15 of the FCC rules (Class A or Class B).
Medical equipment is in accordance with UL 60601-1 and CAN/CSA C22.2 No. 601.1
in regards to electric shock, fire and mechanical hazards
Caution: Federal law (United Stated of America) restricts this device to sale by or on
the order of a licensed healthcare practitioner.
Indicates the legal manufacturer.
Indicates the manufacturing date.
Indicates the entity importing the medical device into the locale.
Important Information