Siemens CLINITEK Status, Operator'S Manual, Page: 127 / 144

10-9
10 Appendices
The instrument complies with the
protection requirements of
EN 61010-1,
EN 50082-1 January 1992,
EN 50081-1 January 1992,
and the safety specifications of
IEC 61010-1 A2 1995.
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 reasonable
protection against harmful
interference when the equipment
is operated in a commercial
environment. The 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.
The instrument is listed by the
Underwriters’ Laboratories (UL) and
the Canadian Standards
Association (CSA) as certified and
complies with the safety standards
specified in UL 61010A-1 and
CSA-C22, No. 1010.1.
Appendix C: Specifications
The instrument is certified as
meeting the EMC requirements and
safety specifications of the In Vitro
Diagnostic Directive
(98/79/EC).