BodyMedia BMSWBT100 Transceiver User Manual BMSWBTBP Literature

BodyMedia, Inc. Transceiver BMSWBTBP Literature

Contents

Users Manual 2

Rev 1 – Dec 04
BioTransceiver for Blood Pressure Monitoring
Supplemental Instructions
Please consult the Omron® Instruction Manual for instructions on setting up the
monitor and taking a reading.
NOTE: The printer shown in the Omron manual has been replaced with the
BioTransceiver which stores the readings taken and forwards them to any nearby
Wireless Gateway. This enables your monitoring service to immediately receive and
review your readings.
The BioTransceiver should remain plugged into the Omron® Automatic Blood
Pressure Monitor at all times as shown below.
Rev 1 – Dec 04
Certifications
Disclaimer
This product is not intended to be a medical device or a substitute for proper medical
diagnosis, care, or treatment related to your condition. Seek professional consultation if you
have any questions related to the readings provided by this product.
FCC statement
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:
• Reorient or relocate the receiving antenna.
• Increase the separation between the equipment and receiver.
• Connect the equipment into an outlet on a circuit separate from the receiver.
• Consult the dealer or an experienced radio/TV technician for help.
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.
CAUTION: Changes or modifications to this equipment not expressly approved by the party responsible
for compliance could void the user's authority to operate the equipment.
FCC 47CFR 15C TCB - 47 CFR Part 15 Subpart C Intentional Radiator Certification Test
FCC 47CFR 15B clB - 47 CFR Part 15 Subpart B Unintentional Radiator Class B Verification
IEC 60601-1-1 (2000-12) - Medical Electrical Equipment - Part 1-1: General Requirements for Safety -
Collateral Standard: Safety Requirements for Medical Electrical Systems Second Edition

Navigation menu