Instructions Manual
Rev 2.0 of 02/2016
3/50
Standard applied in this document:
-
98/79/EEC “directive relevant to the In Vitro Medical-Diagnostic Devices (IVD)”
-
EN 61010-1 (CEI 66-5)
“Safety requirements for electrical equipment for measurement,
control laboratory use
– Part1: General requirements”. The instrument is classified in
Class I
-
EN 61326-
1 “Electrical Equipment for Measurement, Control, and Laboratory Use –
Electromagnetic compatibility requirements-
Part 1: General requirements”
-
EN 61326-2-
6 “Electrical Equipment for Measurement, Control, and Laboratory Use –
Electromagnetic compatibility requirements-Part 2-6: In Vitro Diagnostic (IVD) medical
equipment”
-
2006/95/EEC “Low Voltage Directive”
-
2004/108/EEC “Electromagnetic Compatibility Directive”
-
2011/65/EU “Restriction of Hazardous Substances in Electrical and Electronic
Equipment Directive
– RoHS2”
LIST OF MANUAL REVISIONS
APPLICATION OF THE MANUAL
This manual applies to the following models of the VES-MATIC
CUBE
30:
DIESSE Code
Model description
10390
VES-MATIC
CUBE
30
MANUAL
REVISIONS
VERSION SW VES-
MATIC CUBE 30
DESCRIPTION OF MODIFICATION
0.00 of 10/09 2.06
of
10/09
Initial revision
1.00 of 03/10 2.06
of
10/09
Restyling of the document after its creation by the research
department
1.01 of 07/10 2.06
of
10/09
Changed the customer care address with those of the technical
support
1.02 of 11/10 2.06
of
10/09
Adding of the plate unlocked procedure
1.03 of 02/11 2.06
of
10/09
The Annex about warranty is deleted
1.04 of 11/11 2.17
of
11/11
Modified only the German version as requested by a customer
1.05 of 01/12 2.17
of
11/11
Changed the EC Declaration and deleted the references to
Customer Care
1.06 of 10/14 3.00
of
10/14
Changed software release 3.0
2.00 of 02/16 3.00
of
10/14
Complete restyling
Содержание VES-MATIC CUBE 30
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