Rad-5/5v Safety Information, Warnings and Cautions
www.masimo.com 13 Masimo
Compliance Warnings and Cautions
WARNING: Any changes or modifications not expressly approved by Masimo shall void the
warranty for this equipment and could void the user’s authority to operate the equipment.
WARNING: Per RSS-Gen, Section 8.4 This device complies with Industry Canada license-
exempt RSS standard(s). Operation is subject to the following two conditions: (1) this
device may not cause interference, and (2) this device must accept any interference,
including interference that may cause undesired operation of the device. Per RSS-Gen, Radio
apparatus shall comply with the requirements to include required notices or statements to
the user of equipment with each unit of equipment model offered for sale.
CAUTION: Disposal of Product: Comply with local laws in the disposal of the device and/or
its accessories.
Note: Use Rad-5/5v in accordance with the Environmental Specifications section in the
Operator's Manual.
Note: 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.
Note: This equipment has been tested and found to comply with the limits for medical
devices to the IEC 60601-1-2---, Medical Device Directive 93/42/EEC. These limits are
designed to provide reasonable protection against harmful interference in a typical medical
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 other devices in the vicinity. However, there is no guarantee that interference will not
occur in a particular installation. If this equipment does cause harmful interference to other
devices, which 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 device.
Increase the separation between the equipment.
Consult the manufacturer for help.
Note: This equipment has been tested and found to comply with the Class B limits for
medical devices according to the EN 60601-1-2: 2007, Medical Device Directive 93/42/EEC.
These limits are designed to provide reasonable protection against harmful interference in
all establishments, including domestic establishments.
Note: In order to maintain compliance with FCC regulations, shielded cables must be used
with this equipment. Operation with non-approved equipment or unshielded cables is likely
to result in interference to radio and TV reception. The user is cautioned that changes and
modifications made to the equipment without the approval of manufacturer could void the
user's authority to operate this equipment.
Note: To satisfy RF exposure requirements, this device and its antenna must not be co-
located or operating in conjunction with any other antenna or transmitter.
Note: This Class B digital apparatus complies with Canadian ICES-003.
Note: This device complies with Industry Canada license-exempt RSS standard(s).
Operation is subject to the following two conditions: (1) this device may not cause
interference, and (2) this device must accept any interference, including interference that
may cause undesired operation of the device.
To Next Page
Loading...
Need help?
General
