Fcc Notice; Modification; Cables; Rf Exposure Statement - Philips CliniScape MCA 104 Series User Manual

Mobile clinical assistant
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1.3 FCC Notice

This equipment has been tested and found to comply with the limits for a class B digital device, pursuant to Part
15 of FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a
residential installation.
This equipment generates, uses and can radiate radio frequency energy and, if not installed and used in
accordance with the instructions, may cause harmful interference to radio communications.
However, there is no guarantee that interference will not occur in a particular installation.
If this equipment does cause harmful interference to radio or television reception, while can be determined by
turning the equipment Off and On, the user is encouraged to try to correct the interference by one or more of
the following measures.
- Reorient or relocate the receiving antenna.
- Increase the separation between the equipment and receiver.
- Connect the equipment into an outlet on a circuit different from that to which the receiver is connected.
- Consult the dealer or an experienced radio TV technician for help.
1.3.1

Modification

The FCC requires the user to be notified that any changes or modifications made to this device that are not
expressly approved by the manufacturer may void the user's authority to operate the equipment.
1.3.2

Cables

Connections to this device must be made with shielded signals cables with metallic RFI/EMI connector hoods to
maintain compliance with FCC Rules and Regulations.

1.4 RF Exposure Statement

This device complies with FCC RF radiation exposure limits set forth an uncontrolled environment. This device
has been tested for typical lap-held operations with the device contacted directly to the human body to the back
side of the CliniScape. To mantain compliance with FCC exposure compliance requirements, follow the
instructions described in this User Manual. The device and its antenna(s) must not be co-located or operating in
conjunction with other antenna or transmitter. The availability of some specific channels and/or operational
frequency bands are country dependent and are firmware programmed at the factory to match the intended
destination. The firmware setting is not accessible to the end user.
In order to comply with SAR limits established in the ANSI/IEEE C95.1 standards, it is recommended that the
integrated antenna is positioned more than 1.5cm from your body or from nearby person during extended
periods of operation. If the antenna is positioned less than 1.5cm (0.6 inches) from the user, it is recommended
that the user limit the exposure time.

1.5 Approved for medical applications

The CliniScape meets the medical safety requirements EN/IEC 60601-1, UL 60601-1, CAN/CSA-C22.2 No.
601.1-M90 and electromagnetic requirements EN/IEC 60601-1-2, EN301 489-1/-3/-17, EN 300 328, EN 301 893,
EN 300 330-1, CFR 47 part 15
Do not use the CliniScape AC adapter for other equipment. This can generate heat
or fire.
Do not use other AC adapters with the CliniScape rather then the one supplied with
it.
When using a display for long and continuous periods of time, rest your eyes for
approximately five minutes every hour. Failing to rest your eyes can cause eye strain,
headaches and other discomforts.
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Cliniscape cmca10

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