GE HEALTHCARE Typhoon FLA 7000 User Manual page 8

1 Introduction
1.2 Regulatory information
CE Conformity
This product complies with the European directives listed in the table, by fulfilling the
corresponding harmonized standards. A copy of the Declaration of Conformity is available
on request.
Directive
2006/42/EC
2006/95/EC
2004/108/EC
CE Marking
The CE marking and the corresponding Declaration of Conformity is valid for the
instrument when it is:
•
•
•
•
Note:
8
used as a stand-alone unit, or
connected to other CE marked GE Healthcare instruments, or
connected to other products recommended or described in the user documentation,
and
used in the same state as it was delivered from GE Healthcare, except for alterations
described in the user documentation.
This equipment has been tested and found to comply with the limits
for a Class A digital device, pursuant to Part 15 of the FCC Rules. These
limits are designed to provide reasonable protection against harmful
interference when the equipment is operated in a commercial
environment. This equipment generates, uses, and can radiate radio
frequency energy and, if not installed and used in accordance with the
instruction manual, may cause harmful interference to radio
communications. Operation of this equipment in a residential area is
likely to cause harmful interference in which case the user will be
required to correct the interference at his own expense.
This Class A digital apparatus complies with Canadian ICES-003. Cet
appareil numerique de la class A est conforme a la norme NMB-003
du Canada.
Title
Machinery Directive (MD)
Low Voltage Directive (LVD)
ElectroMagnetic Compatibility (EMC) Directive
Typhoon FLA 7000 User Manual 28-9607-62 AC