Ultrasound Technologies PD1 series, Руководство по обслуживанию

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Ultrasound Technologies Ltd
1.3
5 3
CE Mark
This product complies with the essential requirements of the European Council Directive 93/42/EEC relating to Medical
Devices.
0120
1.4
5 4
Guidelines for identifying and resolving adverse EMC conditions
This product is classified as a Class A Group 1 type of product according to EN55011.
Emissions
Care has been taken through the design and manufacturing process to minimise the EM emissions, which may be
produced by this equipment. However, in the unlikely event that the unit causes an EM disturbance to adjacent
equipment, we suggest that the procedure is carried out ‘out of range’ of the affected equipment.
Immunity
If the user has any doubt regarding the units EM immunity during routine operation, we suggest that the source of EM
disturbance is identified and it’s emissions reduced. If there is any doubt regarding the identification and resolution of
adverse EM conditions, contact Ultrasound Technologies Ltd directly who will advise on the situation. The address
can be found in the front of this manual.
©Ultrasound Technologies Ltd Page 3 of 32
PD1 / FT120 service manual Issue 3 January 2007