Agilent Regulatory Compliance Statement; Ce Compliance; Electromagnetic Compatibility - Agilent Technologies NovoCyte Quanteon Operator's Manual

Prologue
liable for any claims related to or resulting from buyer/user's failure to install and
maintain virus protection.
Do not use the instrument, workstation, and other parts supplied by Agilent
WARNING
Technologies in an oxygen-enriched atmosphere.
Do not use the instrument, workstation, and other parts supplied by Agilent
WARNING
Technologies with flammable liquid/explosive gas or reagents.
Do not use the expired consumables and reagents.
WARNING

Agilent Regulatory Compliance Statement

CE Compliance

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, etc. 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.

Electromagnetic Compatibility

This product conforms to the following regulations on Electromagnetic
Compatibility (EMC) and Radio Frequency Interference (RFI):
NovoCyte Quanteon Flow Cytometer Operator's Guide 23