FCC compliance
This device complies with part 15 of the FCC Rules. Operation is subject to the following
two conditions: (1) This device may not cause harmful interference, and (2) this device
must accept any interference received, including interference that may cause undesired
operation.
The user is cautioned that any changes or modifications not expressly approved
by GE Healthcare could void the user’s authority to operate the equipment.
Note:
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 rea-
sonable protection against harmful interference when the equipment is operated in a
commercial environment. This equipment generates, uses, and can radiate radio frequen-
cy 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 re-
quired to correct the interference at his own expense.
Environmental conformity
This product conforms to the following environmental requirements.
TitleRequirement
Waste Electrical and Electronic Equipment (WEEE) Directive2012/19/EU
Packaging and Packaging Waste Directive and amendment94/62/EC and
2004/12/EC
Administration on the Control of Pollution Caused by Electronic
Information Products, China Restriction of Hazardous Sub-
stances (RoHS)
ACPEIP
Registration, Evaluation, Authorization and restriction of
CHemicals (REACH)
Regulation (EC)
No 1907/2006
Regulatory compliance of
connected equipment
Any electrical equipment connected to ÄKTA ready should meet the safety requirements
of EN/IEC 61010-1, or relevant harmonized standards. Within EU, connected equipment
must be CE marked.
ÄKTA ready Operating Instructions 28960345 AD 11
1 Introduction
1.2 Regulatory information
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