TMA Grand Master 2.0 – User’s Guide Declaration Of Conformity
Declaration Of Conformity
3DHISTECH Ltd. declares that the product TMA Grand Master is designed and produced with
consideration of specified requirements according to the IEC 61326-2-6:2005 standard, and conforms
to the directives and other standards listed below:
IEC 61010-1:2001 (ed. 2), “Safety requirements for electrical equipment for measurement, control,
and laboratory use – Part 1: General requirements”
IEC 61010-2-101:2002 (ed. 1), “Safety requirements for electrical equipment for measurement,
control and laboratory use – Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical
equipment”
DIN EN 55011:2009, Class B, “Limits and methods of measurement of radio disturbance
characteristics of industrial, scientific, and medical (ISM) radio-frequency equipment”
Conformity with Directive 98/79/EC is documented by the TMA Grand Master -label.
This product has been tested to the requirements of CAN/CSA-C22.2 No. 61010-1, second
edition, including Amendment 1, or a later version of the same standard incorporating the same level
of testing requirements.
Further information may be obtained from the manufacturer:
3DHISTECH Ltd.
29-33 Konkoly-Thege Miklos street, Building 6
1121 Budapest – HUNGARY
November 5, 2013 – Rev. 1 3DHISTECH Ltd. 6(72)
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