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Safety and regulatory compliance
CE compliance
Electromagnetic compatibility
G5562A, G5563A Bravo Platform Safety and Installation Guide
The Bravo Platform, when completely assembled with the liquid-handling head, the
light curtain, and other components specified in the Declaration of Conformity,
complies with the applicable EU Directives and bears the CE marking. The Bravo device
alone, without the specified components, is considered a partly completed machine. In
this case, the device has no CE marking and comes with a Declaration of Incorporation,
because it is intended to be incorporated into a compliant system.
See the Declaration of Conformity or Declaration of Incorporation, as applicable, for
details.
Your Agilent instrument has been designed to comply with the requirements of the
applicable directives of the European Union, such as Electromagnetic Compatibility
(EMC) Directive, Low Voltage Directive (LVD), Machinery Directive (MD), RoHS Directive,
and so forth. Agilent has confirmed that each product complies with the relevant
Directives by testing samples against the harmonized EN (European Norm) standards
published on the Official Journal of the European Union (OJEU). Proof that a product
complies with these directives is indicated by
•
The CE Marking appearing on the rear of the product, and
•
The documentation package that accompanies the product containing a copy of
the Declaration of Conformity. The Declaration of Conformity is the legal
declaration by Agilent that the product complies with the relevant directives listed
above, and shows the EN standards to which the product was tested to
demonstrate compliance.
This product conforms to the following regulations on Electromagnetic Compatibility
{EMC) and Radio Frequency Interference {RFI):
•
CISPR11/EN 55011: Group 1, Class A
•
IEC/EN 61326-1
•
AUS/NZ
•
Canada ICES-001 (This ISM device complies with Canadian ICES-001. Cet appareil
ISM est conforme a la norme NMB-001 du Canada).
Group 1 ISM equipment: group 1 contains all Industrial, Scientific and Medical (ISM)
equipment in which there is intentionally generated and/or used conductively coupled
radio-frequency energy that is necessary for the internal functioning of the equipment
itself.
Class A equipment is equipment suitable for use in all establishments other than
domestic and those directly connected to a low voltage power supply network which
supplies buildings used for domestic purposes.
This device complies with the requirements of CISPR11, Group 1, Class A as radiation
professional equipment. Therefore, there may be potential difficulties in ensuring
electromagnetic compatibility in other environments, due to conducted as well as
radiated disturbances.
1 Safety guidelines
Safety and regulatory compliance
3
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