Canada; International; Regulatory Information; Electromagnetic Emissions/Immunity - Kodak Point-of-Care CR 120 Hardware Manual

Safety and Regulatory Information

Canada

International

Regulatory Information

Electromagnetic
Emissions/Immunity
1-6
CAN/CSA 22.2 No. 601.1-M90 - Medical Electrical Equipment (R2001)
CAN/CSA 22.2 No. 601.1S1-94 - Supplement No. 1-94 to Medical Electrical
Equipment (R1999)
CAN/CSA 22.2 No. 601.1B-90 - Amendment 2 to Medical Electrical Equipment
(R2002)
IEC 60601-1: 1988, +A1 (1991), +A2 (1995) Medical Electrical Equipment
IEC 60825 - 1: 1993 +A1:1997 + A2:2001 Safety of Laser Products.
The Product conforms to the following safety standards: IEC 60601-1:2001,
IEC 60601-2:2001 Medical Electrical Equipment General Requirements for
Safety; EN 60601-1-2:2001 Safety of Laser Products - Part 1: Equipment
Classification, Requirements and User's Guide; IEC 60825-1 Safety of Laser
Products.
Electromagnetic Compatibility Precautions
1.
Medical electrical equipment requires special precautions regarding
electromagnetic compatibility (EMC). Medical equipment must be
installed and put into service according to the EMC information provided
in the following documentation.
Communications Equipment
2.
Portable and mobile radio frequency (RF) communications equipment
can affect medical electrical equipment EMC performance.
Replacement of Cables, Accessories or Transducers
3.
The use of cables, accessories or transducers other than those specified
below with the exception of transducers or cables sold by the
manufacturer of the equipment as replacement parts for internal
components, may result in increased emissions or decreased immunity
of the medical equipment.
Other Equipment
4.
The CR 120/140 scanner should not be used adjacent to or stacked with
other equipment. If adjacent or stacked use is necessary, the scanner
should be observed to verify normal operation in the configuration in
which it will be used.
Cable, Accessory and Transducer Information for the CR 120/140
5.
6H8044