User Manual

ManualsBrandsBodyMedia ManualsElectronicsSenseWear (R) biotransceiver

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Sending a Reading to SenseWear

armband

Sending a Reading to SenseWear

wireless gateway

Place t he bl ood pr essure monit or and SenseWear

biotransceiver wit hin 5 met ers (15 f eet )

of t he SenseWear

wirel ess gat eway.

Ensure t he biot ransceiver is plugged int o t he print er port of t he blood pressure monit or

(ﬁ gure 2).

Please consult the SenseWear

wirel ess gat eway Operat ing Manual f or furt her instr uct ions

Turn t he power on t o t he blood pressure monit or.

Once t he blood pressure moni t or displ ays zero, f oll ow Omron’s procedures for t aking

a reading.

Turn t he blood pressure monit or power off t o send t he reading t o t he biotransceiver. As

soon as ret rieval t he is complet e, t he biot ransceiver will send dat a t o t he wireless gat e-

way. The LED on t he biot ransceiver will bl ink green when successful and red if t he t ransf er

failed.

Pat ent s and pat ent s pending. The BodyMedia

biotransceiver is covered by one or more of t he

fol lowing pat ent s when used wit h a BodyMedia

armband (e. g., SenseWear

armbands and

bodybugg™ armbands): Unit ed St ates Pat . Nos.: 6,527,711, 6, 595, 929, 6, 605, 038, 7,020, 508;

European Pat ent Nos. : 1, 292, 217, 1, 292, 218; and various worldwide pat ent s pending.

SenseWear

and BodyMedia

are regist ered trademarks of BodyMedia, Inc. Omron is a regist ered

t rademark of Omron Tat eishi Elect ronics Co.

FCC Statement

NOTE: This equipment has been t ested and f ound t o comply wit h t he l imit s f or a Class B di git al device,

pursuant t o Part 15 of t he FCC Rul es. These limit s are designed to provide reasonable prot ect ion against

har mful int er f erence in a resident ial inst al lat ion. This equipment generat es, uses, and can radiat e radio

fr equency ener gy and, if not installed and used in accordance with t he inst r uct ions, may cause harmf ul

int er f erence t o radio communi cat ions. However, t here is no guar ant ee t hat int er f erence wi ll not occur

in a part icular inst al lat ion. If t his equipment does cause har mf ul int er f erence t o radio or t elevision

recept ion, which can be det ermined by turning t he equipment of f and on, t he user is encouraged t o t ry

t o correct the int erf erence by one or more of t he fol lowing measures:

Reorient or r el ocat e t he receiving antenna.

Increase t he separat ion bet ween the

equipment and receiver.

Connect t he equipment int o an out let on a circuit separat e from t he receiver.

Consul t t he dealer or an experi enced radio/ TV t echnician f or help.

This device complies wit h part 15 of t he FCC Rul es. Operat ion is subj ect t o t he following t wo condi-

t ions: (1) This device may not cause harmf ul i nt erference, and (2) t his devi ce must accept any interfer-

ence received, incl uding int erf erence t hat may cause undesired operat ion.

•

FCC 47CFR 15C TCB - 47 CFR Part 15 Subpart C

Intent ional Radiat or

Cer t iﬁ cat ion Test

FCC 47CFR 15B cl A - 47 CFR Part 15 Subpart B Unin-

t ent ional Radiat ors Class A Veriﬁ cat ion

UL 60601-1 - UL Standard f or Saf et y Medical El ect r i -

cal Equipment , Part 1:

Gener al Requirement s for Saf ety First Edit ion

CENELEC EN 60601-1-2 - 2001 - Medical El ect rical

Equipment Part 1-2: General Requi r ement s f or Safet y

- Collat er al St andard: Electromagnet ic Compatibilit y

- Requirements and Tests IEC 60601-1-2: 2001

CENELEC EN 60601-1-1 - Medical El ect rical Equip-

ment - Part 1: General Requirement s for Saf et y -

Col l at eral St andar d: Saf et y Requirements f or Medical

Elect rical Syst ems.

CAN/ CSA-C22. 2 No.606. 1-M90

ETSI EN 301 489-1 - Electromagnet ic Compatibilit y

and Radio Spect rum Mat t ers (ERM); El ect r oMagnetic

Compatibilit y (EMC) Standard f or Radi o Equipment

and Services; Par t 1: Common Technical Require-

ment s V1. 3. 1

ETSI EN 301 489-3 - (Draft ) Elect romagnetic Compat .

and Radio Spect rum Mat t ers (ERM); Har monized EN

for Elect roMag. Compat ibi l it y (EMC) of Radio Comms.

Equip. & Sr vs. ; Pt . 3: Speciﬁ c Conditions for Short -

Range Devices (SRD) Operat ing on Freqs Between 9

KHz and 40 GHz V1.3. 1

ETSI EN 300 440-1 V1. 3. 1 (2001-07) El ect romag-

net ic compat ibilit y and Radio spect rum Mat t ers

(ERM);Short range devices; Radio equipment t o be

used in t he 1 GHz t o 40 GHz frequency range

Once t he blood pressure moni t or displ ays zero, f oll ow Omron’s procedures for t aking

a reading.

Turn t he blood pressure monit or power off t o send t he reading t o t he biotransceiver. As

soon as ret rieval is complet e, t he biot ransceiver will send dat a t o t he armband. The LED

on t he biotransceiver will bli nk green when successf ul and red if t he transfer fail ed.

The armband will also beep and vibrat e once t he transfer is successfully compl eted.