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TMA Grand Master 2.6 – 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 i
n 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 and
ANSI/UL 61010-1 by TÜV Rheinland.
Further information may be obtained from the manufacturer:
3DHISTECH Ltd.
3 Öv street
1121 Budapest – HUNGARY
December 9, 2016 – Rev. 1
3DHISTECH Ltd.
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