Note - HoMedics HL858DM Instruction Manual

Automatic upper arm blood pressure monitor
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Note

*Note
This equipment has been tested and found to comply with the limits for a Class B digital 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 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, 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:
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 the 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.
CAUTION:
To assure continued FCC compliance:
Any changes or modifications not expressly approved by the grantee of this device could void the user's authority
to operate the equipment.
RF exposure warning
1.
The equipment complies with FCC RF exposure limits set forth for an uncontrolled environment.
2.
The equipment must not be co-located or operation in conjunction with any other antenna or transmitter.
FCC Label Compliance Statement:
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!
"Changes or modifications not expressly approved by the manufacturer could void the user's authority to
operate the equipment"
HL858DM essential performance per IEC 80601-2-30 additional
essential performance requirements:
201.12.1.102 Limits of the error of the manometer from
environmental conditions
Over the temperature range of 5 °C to 40 °C (41 °F ~ 104 °F ) and the
relative humidity range of 15 % to 93 %(non-condensing), the
maximum error for the measurement of the CUFF pressure at any point
of the NOMINAL measurement range shall be less than or equal to ± 3
mmHg (± 0.4 kPa) or 2 % of the reading, whichever is greater.
201.12.1.107 Reproducibility of the blood pressure determination
The laboratory Reproducibility of the BLOOD PRESSURE
DETERMINATION of the AUTOMATED SPHYGMOMANOMETER shall be
less than 3 mmHg (0.4 kPa).
35
VER: A001 202203

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