BodyMedia FIT Armband and Display Manual
BodyMedia FIT Armband and Display Manual
Regulatory Statement
FCC Declaration of Conformity
– We, BodyMedia, Inc., One Gateway Center, 420 Fort Duquesne
Boulevard, Suite 1900, Pittsburgh, PA 15222, declare under our sole responsibility that the
products, BodyMedia, Inc. and BodyMedia® Armbands (Model MF) and BodyMedia® Display
(Model DD100) comply 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.
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 instruc-
tions, 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 follow-
ing 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.
•
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.
RF Exposure information: See 2.1093 of the FCC Rules
This product is a Type B Applied Part complying with the specified requirements of the Standard
to provide protection against electric shock, particularly regarding allowable Leakage Current.
This Class B digital apparatus complies with Canadian ICES-003.
Cet apareil numèrique de la classe B est conforme à la norme NMB-003 du Canada.
Radio Frequency: 2.4 GHz
Transmitter output power: Model MF <1mW
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Models MF and DD100:
FCC 47CFR Part 15 Subpart B Unintentional Radiator Tests
FCC 47CFR Part 15 Subpart C Intentional Radiator Tests
ETSI EN 301 489-1 with ETSI EN 301 489-17 (Article 3.1(b) of R&TTE Directive) 2.4GHz.
ICES-003 Tests
EN 60601-1-2: Medical electrical equipment – Part 1-2: General requirements for safety – Collat-
eral standard: Electromagnetic compatibility – Requirements and tests
IEC 60601-1-2 – Medical electrical equipment – Part 1-2: General requirements for safety – Collat-
eral standard: Electromagnetic compatibility – Requirements and tests
UL 60601-1– Medical Electrical Equipment; Part 1 General Requirements for Safety
CSA C22.2 No. 60601-1– Medical Electrical Equipment; Part 1 General Requirements for Safety
EN 60601-1- Medical Electrical Equipment; Part 1 General Requirements for Safety
IEC 60601-1- Medical Electrical Equipment; Part 1 General Requirements for Safety
RoHS requirements.
RSS210 Tests – Industry Canada emissions requirements
ETSI EN 300 440-1 and ETSI EN 300 440-2
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