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iHealth BP5 Instructions page 18

Systeme de monitorage de tension arterielle sans fils
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IMPORTANT INFORMATION REQUIRED BY THE FCC
This device complies with Part 15 of the FCC Rules. Its operation is subject to the
following two conditions:
• This device may not cause harmful interference.
• This device must accept any interference received, including interference that may
cause undesired operation.
Changes or modifications not expressly approved by iHealth Lab Europe. would
void the user's authority to operate the product.
Note: This product has been tested and found to comply with the limits for a Class B dig-
ital device, pursuant to Part 15 of the FCC Rules. These limits are designed to provide
reasonable protection against harmful interference in a residential installation. This
product 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 product does cause harmful interference to radio or televi-
sion reception, which can be determined b
is encouraged to try to correct the interference by one or more of the following meas-
ures:
• Reorient or relocate the receiving antenna.
• Increase the separation between the equipment and receiver.
• Connect the equipment into an outlet on a circuit
ceiver is connected.
• Consult the dealer or an experienced radio/TV technician for help.
This product complies with Industry Canada. IC: RSS-210 IC NOTICE.
This device complies with Industry Canada license-exempt RSS standard(s). Opera-
tion is subject to the following two conditions:
• This device may not cause interference.
• This device must accept any interference, including interference that may cause
undesired operation of the device.
This product is approved in accordance to R&TTE directive transmitter.
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rent from that to which the re-

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