TERRAILLON TENSIOSMART User Manual [nl]

USER MANUAL | GUIDE D’UTILISATION

NL Handleiding|IT Manuale di istruzion|ES Manual de instrucciones

DE Bedienungsanleitung|PT Manual de instruções

www.terraillon.com

Made for / Compatibilité

®

iPhone
iPod

iPad
iPad

4S & +

®

Touch 5th generation

®

3 & +

®

Mini & +

Android 4.4 & +
Bluetooth Smart 4.0 / Bluetooth Smart Ready

iPhone is registered trademark of Apple Inc.

Android is a trademark of Google Inc.

®

The Bluetooth

word mark and logos are registered trademarks

owned by Bluetooth SIG, Inc.

Other trademarks and trade names are those of their respective owners.

2

EN TERRAILLON CONNECTED BLOOD PRESSURE MONITOR

INSTRUCTION MANUAL ............................................................................ 4

FR TENSIOMÈTRE CONNECTÉE TERRAILLON

NOTICE D’UTILISATION ............................................................................. 8

NL TERRAILLON BLOEDDRUKMETER

HANDLEIDING ........................................................................................ 12

IT SFIGMOMANOMETRO TERRAILLON

MANUALE DI ISTRUZIONI ........................................................................ 16

ES TENSIÓMETRO TERRAILLON

MANUAL DE INSTRUCCIONES ............................................................... 20

DE BLUTDRUCKMESSGERÄT TERRAILLON

BEDIENUNGSANLEITUNG ....................................................................... 24

PT MONITOR DE PRESSÃO SANGUINEA TERRAILLON

MANUAL DE INSTRUÇÕES ..................................................................... 28

3

EN

Thank you very much for selecting the Terraillon Arm Blood Pressure Monitor
TENSIOSMART.

This unit allows you to monitor your blood pressure. This device is not
intended to be a diagnostic device. Always contact your doctor for

!

advice, diagnostic and treatment.

FIND MORE INFORMATION ON

http://www.terraillon.com

PRODUCT OVERVIEW

Start-Stop

User 1

Start-Stop

User 2

Pair-up

LCD display

Cuff

Power socket

On/Off button

Systolic Blood Pressure

Diastolic Blood Pressure

Pulse

Unit

Data transmitting

Low Battery

Time [Hour/Minute - Month/Day]

Irregular Heartbeat Detector

4

FIRST USE

A

Switch the button « on » and press and hold User1 button to set time. Press
button

con rming [TIME] and [DATE], the LCD will display “Done”.

If the battery is low or empty, please recharge it with the authorized adaptor
included in the pack.

B

Download the Terraillon Wellness Coach application.

C

Create your account.

to change the numeral then press User1 button to con rm. After

5

EN

1
2
3

4

1

1

2
3

4

D

Turn on Bluetooth on your Smartphone (Setting > Bluetooth > ON).

E

Press and hold User2 button to start pair-up.

1

1
2

3

4

1
2

1
2
3

4

5

EN

F

1

1

1

1

START MEASURING

A

Tie the cuff

B

Press User1 or User2 button to turn on the monitor, and it will complete the
measurement process automatically

2~3cm

6

1

RECORDS

Press button to access the memory. Press User1 or User2 to recall the measurement
history of each user.

EN

Press and hold button

“dEL ALL”, press button

for 3 seconds to clear the memory. When the LCD display

to conrm.

TIPS FOR MEASUREMENT

Optimal Normal High-normal Mild Moderate Severe

SYS <120 120-129 130-139 140-159 160-179 ≥180

DIA <80 80-84 85-89 90-99 100-109 ≥110

* The blood pressure classication published by World Health Organization

(WHO) and International Society of Hypertension (ISH).

TROUBLESHOOTING

E1 Communication error. Check the app and Bluetooth.
E3 The cuff is not secure. Refasten the cuff.
E10/11 The monitor detected motion while measuring.
E20 Measurement process does not detect the pulse signal
E21 Measure incorrectly.
Eexx A calibration error occurred.
Lo Low Battery. Charge the battery.

WARRANTY & ENVIRONMENT PROTECTION

This product is guaranteed for 2 years against material and manufacturing
defects. During this period, such defects will be repaired free of charge (proof of
purchase must be presented if the scale is under warranty). This warranty does not
cover damage resulting from accidents, improper use or negligence. If you have

a complaint please contact the store where you purchased the product rst.

Waste electrical products should not be disposed of with household waste.
Please recycle where facilities exist. Check with your local authority or
retailer for recycling advice.

7

FR

Nous vous remercions d’avoir choisi le tensiomètre bras TENSIOSMART de
Terraillon.

Cet appareil vous permet de contrôler votre tension artérielle. Il n’a pas
vocation à être un dispositif de diagnostic. Contactez toujours votre

!

médecin pour obtenir tout conseil, diagnostic ou traitement.

BESOIN D’INFORMATION ?

http://www.terraillon.com

APERÇU DU PRODUIT

Marche-Arrêt

Utilisateur 1

Marche-Arrêt

Utilisateur 2

Synchronisation

Écran LCD

Bouton marche/arrêt

Pression artérielle systolique

Pression artérielle diastolique

Pouls

Unité

Données en cours de transmission

Batterie faible

Heure [Heure/Minute - Mois/Jour]

Détecteur de rythme cardiaque irrégulier

Brassard

Branchement
chargeur

8

PREMIÈRE UTILISATION

A

Mettez le bouton en position « marche » puis maintenez enfoncé Utilisateur1
pour accéder au réglage de l’heure. Appuyez sur

puis cliquez sur le bouton Utilisateur1 pour con rmer. Après avoir con rmer
[HEURE] et [DATE], l’écran LCD af chera « Done».

Si la batterie est faible ou vide, branchez le produit sur une prise avec
l’adaptateur fourni.

B

Téléchargez l’application Terraillon Wellness Coach.

C

Créez votre compte sur l’application.

1
2
3

1

4

pour modi er le chiffre

5

1
2

3

4

FR

1
2
3

4

1
2

3
4

D

Activez la fonction Bluetooth sur votre Smartphone (Réglages > Bluetooth > ON).

E

Appuyez sur le bouton Utilisateur2 et maintenez-le appuyé pour démarrer

1

1
2

la synchronisation.

9

FR

F

1

1

1

1

CRÉEZ VOTRE COMPTE SUR L’APPLICATION

A

Attachez le brassard.

B

Appuyez sur Utilisateur1 ou Utilisateur2 pour activer l’appareil. Votre prise de
tension se fera de manière automatique.

2~3cm

10

1

MÉMOIRES

Appuyez sur le bouton pour accéder à la mémoire. Appuyez sur le bouton

Utilisateur1 ou Utilisateur2 pour faire déler l’historique de chaque utilisateur.

FR

En mode rappel de mémoire, appuyez sur le bouton

pendant 3 secondes pour effacer les enregistrements. Lorsque l’écran afche
“dEL ALL”, appuyez sur

pour conrmer

et maintenez-le enfoncé

INDICATIONS POUR LA MESURE

Optimal Normal

SYS <120 120-129 130-139 140-159 160-179 ≥180

DIA <80 80-84 85-89 90-99 100-109 ≥110

* Classication de la tension artérielle par l’Organisation Mondiale de la Santé

(OMS) et la Société Internationale d’Hypertension (ISH).

Normal
à élevé

Moyen Modéré Sévère

DIAGNOSTIC

E1 Erreur de communication; Vériez l’application et le Bluetooth.
E3 Le brassard est mal attaché. Veuillez le remettre correctement.
E10/11 L’appareil a détecté un mouvement pendant la mesure.
E20 Aucun signal de pouls n’a été détecté.
E21 Mesure incorrecte.
Eexx Une erreur d’étalonnage s’est produite.
Lo Batterie faible. Veuillez recharger l’appareil.

GARANTIE ET PROTECTION DE L’ENVIRONNEMENT

Cet appareil est garanti 2 ans contre tout défaut matériel et de fabrication. Au cours
de cette période, ces défauts seront réparés gratuitement (une preuve d’achat doit
être présentée si la balance est sous garantie). Cette garantie ne couvre pas les
dommages provenant d’accidents, d’une mauvaise utilisation ou de négligence.
Si vous avez une réclamation, adressez-vous d’abord au magasin où vous avez
acheté votre produit.

Les déchets de produits électriques ne doivent pas être jetés avec les ordures
ménagères. Les recycler dans les installations prévues à cet effet. Contacter
l’administration locale ou le détaillant pour tout conseil de recyclage.

11

NL

Bedankt om voor de Bloeddrukmeter TENSIOSMART van TERRAILLON te kiezen.

Met deze unit kunt u uw bloeddruk meten. Het apparaat is niet bedoeld
om een diagnose te stellen. Wend u steeds tot uw arts voor advies,

!

diagnose en behandeling.

MEER INFORMATIE OVER

http://www.terraillon.com

OVERZICHT

Gebruiker 1

Gebruiker 2

Koppeling

Lcd-scherm

Polsband

Stopcontact

Aan / uit-knop

Systolische bloeddruk

Diastolische bloeddruk

Hartslag

Unit

Gegevens worden overgedragen

Batterij bijna leeg

Tijd [Uur/Minuut - Maand/Dag]

Detector onregelmatige hartslag

12

EERSTE INSTALLATIE

A

Zet de knop «Aan» en Houd de User1-toets 3 seconden ingedrukt om naar de
tijdinstelmodus te gaan. Druk op
User1 om het te bevestigen. Nadat u [UUR] en [DATUM] hebt bevestigd, verschijnt

de vermelding “Done” op het lcd-scherm schakelt.

Als de batterij bijna leeg is of leeg is, dan kunt u opladen met de bevoegde
adapter meegeleverd in de verpakking.

B

Download de Terraillon Wellness Coach-app.

C

Maak een account aan.

om het cijfer te wijzigen en druk opnieuw op

5

NL

1
2
3

4

1

1

2
3

4

D

Schakel de Bluetooth-functie van uw smartphone in (Instellingen > Bluetooth > AAN).

E

Houd de “Gebruiker 2”-toets om de koppeling te starten.

1

1
2

3

4

1
2

1
2
3

4

13

NL

F

1

1

1

1

BEGINNEN MET METEN

A

De polsband bevestigen.

B

Drukt u op “Gebruiker 1/2”-toets om de meter in te schakelen. Deze zal het

meetproces automatisch voltooien.

2~3cm

14

1

GEGEVENS

Druck op om toegang te krijgen tot het geheugen. Druk op Gebruiker 1 of
Gebruiker 2 om de opgeslagen gegevens te doorbladeren.

NL

Houd in de oproepmodus de

wissen. “dEL ALL” verschijnt op het lcd-scherm, druk opnieuw op

bevestigen.

toets 3 seconden ingedrukt om Gegevens te

om het te

MEETTIPS

Optimaal Normaal

SYS <120 120-129 130-139 140-159 160-179 ≥180

DIA <80 80-84 85-89 90-99 100-109 ≥110

Hoog-

normaal

Licht Matig Ernstig

PROBLEMEN OPLOSSEN

E1 Communicatie fout. Controleer de app en Bluetooth.
E3 De manchet is niet veilig. Weer vast de manchet.
E10/11 De meter detecteerde beweging tijdens het meten.
E20 Het meetproces detecteert geen hartslagsignaal.
E21 Onjuiste meting.
Eexx Er is een ijkingsfout opgetreden.
Lo Batterij bijna leeg. De batterij opladen.

GARANTIE & BESCHERMING VAN HET LEEFMILIEU

Voor dit toestel geldt een garantie van 2 jaar tegen materiaal- en fabricagefouten.
Gedurende deze periode zullen dergelijke defecten gratis gerepareerd worden
(tijdens de garantieperiode moet een bewijs van aankoop worden overgelegd).
Schade veroorzaakt door ongevallen, onjuist gebruik of nalatigheid valt niet onder
de garantie. Als u klachten hebt, dient u zich in eerste instantie te wenden tot de
winkel waar u de monitor heeft gekocht.

Afgedankte elektrische producten horen niet bij het huishoudelijk afval.
Gelieve te recycleren waar mogelijk. Raadpleeg uw lokale overheid of
verkoper voor recyclingadvies.

15

IT

Grazie per aver scelto TENSIOSMART il monitor per la misurazione della pressione
sanguigna TERRAILLON.

L’unità permette di monitorare la pressione del sangue. Il dispositivo
non è pensato come apparecchio di diagnosi. Contattare sempre il

!

proprio medico per consigli, diagnosi e terapia.

TROVATE MAGGIORI INFORMAZIONI SUL

http://www.terraillon.com

IN SINTESI

Utente 1

Utente 2

Sincronizzazione

Display LCD

Bracciale

Presa energia

Pulsante On / Off

Pressione arteriosa sistolica

Pressione arteriosa diastolica

Pulsazioni

Unità

Trasmissione dati

Batteria scarica

Data/ora [Ore/Minuti - Mese/Giorno]

Rilevatore battito cardiaco irregolare

16

PRIMA INSTALLAZIONE

A

Accendere il tasto «on» e mantenere premuto il tasto User1 per 3 secondi
per entrare nella modalità impostazione data/ora. Premere il tasto

modi care il numero e premere nuovamente il tasto Utente 1 per confermare.
Dopo aver confermato [ORA] e [DATA], il display LCD mostra “Done”.

Se la batteria è basso o vuoto, si prega di ricaricarla con l’adattatore
autorizzato incluso nella confezione.

B

Scaricare l’app Terraillon Wellness Coach.

C

Creare un account.

5

IT

per

1
2
3

4

1

1

2
3

4

D

Attivare la funzione Bluetooth sullo Smartphone (Impostazioni > Bluetooth > ON).

E

Tenere premuto il tasto “Utente 2 ” per avviare l’accoppiamento.

1

1
2

3

4

1
2

1
2
3

4

17

IT

F

1

1

1

1

AVVIARE LE MISURAZIONI

A

Fissaggio del bracciale.

B

Premere “Utente1”/”Utente2” per accendere il monitor che completerà

automaticamente la procedura di misurazione.

2~3cm

18

1

REGISTRAZIONI

Premere il tasto per accedere alla memoria. Premere il tasto Utente1 oppure

Utente2 per modicare la disposizione delle registrazioni della cronologia.

In modalità di accesso memoria, tenere premuti contemporaneamente per 3
secondi il tasto

il messaggio “dEL ALL”, premere nuovamente il tasto

SUGGERIMENTI PER LA MISURAZIONE

SYS <120 120-129 130-139 140-159 160-179 ≥180

DIA <80 80-84 85-89 90-99 100-109 ≥110

RISOLUZIONE DEI PROBLEMI

E1 Errore di comunicazione. Controllare l’applicazione e Bluetooth.
E3 Il bracciale non è sicuro. Fissare nuovamente il bracciale.
E10/11 Il monitor ha rilevato un movimento durante la misurazione.
E20 La procedura di misurazione non rileva il segnale del polso.
E21 Misurazione incorretta.
Eexx Si è vericato un errore di calibrazione.
Lo Batteria scarica.

per l’eliminazione delle registrazioni. Lo schermo LCD mostrerà

per confermare.

Ottimale Normale Alto-normale Lieve Moderato Grave

IT

GARANZIA & PROTEZIONE DELL’AMBIENTE

Questo prodotto è garantito per 2 anni contro difetti di materiale e di fabbricazione.
Durante questo periodo, tali difetti saranno riparati gratuitamente (presentare
la prova di acquisto se la bilancia è sotto garanzia). Questa garanzia non copre
i danni derivanti da incidenti, uso improprio o negligenza. In caso di reclamo
contattare il negozio presso cui è stata acquistata il monitor.

I riuti di apparecchiature elettriche non devono essere smaltiti come riuti

domestici. Riciclare dove esistono strutture atte allo scopo. Consultare le
autorità locali o il rivenditore per indicazioni riguardanti il riciclaggio.

19

ES

Muchas gracias por haber elegido el tensiómetro TENSIOSMART de TERRAILLON.

Esta unidad le permite controlar su tensión arterial. Este dispositivo
no ha sido diseñado como dispositivo de diagnóstico. Para recibir
asesoramiento, diagnóstico y tratamiento, consulte siempre a su

!

médico.

ENCONTRAR MÁS INFORMACIÓN SOBRE

http://www.terraillon.com

DESCRIPCIÓN GENERAL

Usuario 1

Sincronización

Usuario 2

Pantalla LCD

Botón de encendido / apagado

Tensión arterial sistólica

Tensión arterial diastólica

Pulso

Unidad

Transmisión de datos

Batería baja

Hora [Hora / minuto - Mes / día]

Detector de latidos irregulares

Toma de
corriente

Manguito

20

INSTALACIÓN INICIAL

A

Cambie el botón «encendido» y mantenga pulsado el botón User1 durante 3
segundos para entrar en el modo de ajuste de hora. Pulse el botón

cambiar el número y vuelva a pulsar el botón Usuario 1 para con rmar. Una
vez con rmados los [TIEMPO] y el [FECHA], en la pantalla LCD aparecerá el

mensaje «Done».

Si la batería está bajo o vacío, por favor recarga con el adaptador autorizado

incluido en el paquete.

Descargue la aplicación Terraillon Wellness Coach.

B

C

Cree una cuenta.

5

ES

para

1
2
3

4

1

1

2
3

4

D

Active la función Blueetooth en su smartphone (Ajustes > Blueetooth > ACTIVADO).

E

Mantenga pulsado el botón “Usuario 2” para iniciar el emparejamiento.

1

1
2

3

4

1
2

1
2
3

4

21

ES

F

1

1

1

1

COMENZAR A MEDIR

A

Fijación del manguito.

B

Pulse “Usuario1”/ “Usuario2” para encender el tensiómetro y este realizará el
proceso de medición de forma automática.

2~3cm

22

1

REGISTROS

Pulse el botón para acceder a la memoria. Pulse el botón Usuario 1 o Usuario 2
para moverse por los registros del historia.

ES

En el modo de consulta de memoria, mantenga pulsados el botón

durante 3 segundos para el eliminación de registros. La pantalla LCD mostrará

el mensaje «dEL All», vuelva a pulsar el botón

para conrmar.

CONSEJOS PARA REALIZAR MEDICIONES

Óptima Normal Normal-alta Leve Moderada Grave

SYS <120 120-129 130-139 140-159 160-179 ≥180

DIA <80 80-84 85-89 90-99 100-109 ≥110

SOLUCIÓN DE PROBLEMAS

E1 Error de comunicacion. Compruebe la aplicación y Bluetooth.
E3 El brazalete no es seguro. Vuelva a ajustar el brazalete.
E10/11 El tensiómetro ha detectado movimiento durante la medición.
E20 El proceso de medición no detecta la señal de pulso.
E21 Medición incorrecta.
Eexx Error de calibración.
Lo Batería baja. Recargar la batería.

GARANTÌA & PROTECCIÓN MEDIOAMBIENTAL

El producto está garantizado por un período de dos años contra todo defecto

de material y de fabricación. Durante dicho período, los problemas de este

tipo se repararán gratuitamente, previa presentación de un justicante de

compra. La garantía no cubre los daños resultantes de accidentes, uso indebido
o negligencia. Si tiene una reclamación, le rogamos se ponga en contacto, en
primer lugar, con la tienda en la que adquirió el producto.

Los productos eléctricos no deben desecharse con la basura doméstica.
Recíclelos en las instalaciones disponibles. Consulte a las autoridades
locales o al comerciante para informase sobre el reciclado.

23

DE

Vielen Dank, dass Sie sich für ein TERRAILLON Blutdruckmessgerät TENSIOSMART
entschieden haben.

Dieses Gerät ermöglicht Ihnen die Kontrolle Ihres Blutdrucks. Es ist nicht
für diagnostische Zwecke bestimmt. Für Diagnose, Rat und Behandlung

!

sollten Sie stets Ihren Arzt aufsuchen.

MEHR INFORMATIONEN FINDEN SIE

http://www.terraillon.com

FUNKTIONEN

Benutzer 1

Synchronisation

Benutzer 2

LCD-Display

Manschette

Steckdose

Ein / Aus-Taste

Systolischer Blutdruck

Diastolischer Blutdruck

Puls frequenz

Gerät

Datenübertragung

Batterie schwach

Zeit [Stunde/Minute - Monat/Tag]

Melder für unregelmäßigen Herzschlag

24

ERSTINSTALLATION

A

Schalten Sie den Knopf «auf» und halten Sie die User1-Taste 3 Sekunden lang
gedrückt, um den Zeiteinstellungsmodus aufzurufen. Drücken Sie die Taste
um die Zahl zu ändern und Drücken Sie erneut Benutzer 1, um die Zahl zu
bestätigen. Nachdem Sie [ZEIT] und [DATUM]bestätigt haben, erscheint die

Meldung „Done“ auf dem Display.

Wenn die Batterie schwach oder leer ist, laden Sie ihn bitte mit dem
autorisierten Adapter in der Packung enthalten.

B

Laden Sie die App Terraillon Wellness Coach herunter.

C

Legen Sie ein Konto an.

5

DE

1
2
3

4

1

1

2
3

4

D

Aktivieren Sie die Bluetooth-Funktion auf Ihrem Smartphone (Einstellungen >

1

1
2

3

4

1
2

Bluetooth > ON).

E

Halten Sie die “Benutzer 2” -Taste um das Koppeln zu aktivieren.

1
2
3

4

25

DE

F

1

1

1

1

ERSTE MESSUNGEN

A

Anbringen der Manschette.

B

Drücken Sie “Benutzer1”/ “Benutzer2”--Taste, um das Gerät einzuschalten.

Dann erfolgt die Messung automatisch.

2~3cm

26

1

DATEN

Drücken Sie , um auf den Speicher zuzugreifen. Drücken Sie Benutzer 1 oder
Benutzer 2, um die gespeicherten Ergebnisse einzusehen.

DE

Halten Sie im Speicher-Aufruf-Modus gleichzeitig die Taste

gedrückt, um die Daten zu löschen. Erscheint „dEL ALL“ im Display, drücken Sie

erneut

, um zu bestätigen.

3 Sekunden lang

TIPPS ZUR MESSUNG DES BLUTDRUCKS

Optimal Normal Hoch-normal

SYS <120 120-129 130-139 140-159 160-179 ≥180

DIA <80 80-84 85-89 90-99 100-109 ≥110

Leichte

Hypertonie

Mittlere

Hypertonie

Schwere

Hypertonie

PROBLEMLÖSUNG

E1 Kommunikationsfehler. Überprüfen Sie die App und Bluetooth.
E3 Die Manschette ist nicht sicher. Befestigen Sie wieder die Manschette.
E10/11 Das Gerät hat während der Messung eine Bewegung erkannt.
E20 Während der Messung wurde kein Pulssignal erfasst.
E21 Falsche Messung.
Eexx Ein Kalibrationsfehler ist aufgetreten.
Lo Niedriger Batteriestatus. Lade die Batterie auf.

GARANTIE & UMWELTSCHUTZSYMBOL

Für dieses Produkt besteht eines 2-Jahres-Garantie gegen Material- und
Fabrikationsfehler. Während dieses Zeitraums werden diese Fehler kostenlos
repariert (wenn die Waage unter Garantie steht, muss ein Kaufnachweis vorgelegt
werden). Diese Garantie deckt keine Schäden, die aus Unfällen, unsachgemäßer
Verwendung oder Nachlässigkeit entstehen. Bei Reklamationen wenden Sie sich
bitte an das Geschäft, in dem Sie die Blutdruckmessgerät erworben haben.

Elektrische Geräte getrennt von Hausmüll entsorgen. Bitte nach Möglichkeit
recyceln. Erkundigen Sie sich bei Ihrem Händler oder Ihrer Gemeinde nach
Recyclingmöglichkeiten.

27

PT

Muito obrigado por escolher TENSIOSMART o Monitor de Pressão Sanguínea
TERRAILLON.

Esta unidade permite-lhe controlar a sua pressão sanguínea. Este
dispositivo não se destina a ser utilizado como dispositivo de diagnóstico.
Contacte sempre o seu médico relativamente a diagnósticos,

!

aconselhamento e tratamento.

OBTENHA MAIS INFORMAÇÕES SOBRE

http://www.terraillon.com

VISÃO GERAL

Utilizador 1

Ecrã LCD

Bracelete

Tomada de
alimentação

Utilizador 2

Sincronização

Pressão Sanguínea Sistólica

Pressão Sanguínea Diastólica

Batimentos cardíacos

Unidade

Dados em transmissão

Pilha Fraca

Tempo [Hora/Minuto - Mês/Dia]

Detetor de batimentos cardíacos irregulares

28

Botão On / Off

PRIMEIRA INSTALAÇÃO

A

Mudar o botão «on» e prima e mantenha premido o botão User1 durante

3 segundos, para entrar no Modo de De nição do Tempo. Prima o botão
para alterar o número e prima novamente o botão Utilizador 1 para con rmar.
Depois de con rmar os [HORA] e [DATA], o LCD apresenta a mensagem “Done”.

Se a bateria estiver baixo ou vazio, por favor, recarregá-lo com o adaptador

autorizado incluído no pacote.

B

Descarregue a aplicação Terraillon Wellness Coach.

C

Crie uma conta.

5

PT

1
2
3

4

1

1

2
3

4

D

Active a função Bluetooth no Smartphone (De nições > Bluetooth > Ligado).

E

Mantenha premido o botão “Utilizador 2” para iniciar a sincronização.

1

1
2

3

4

1
2

1
2
3

4

29

PT

F

1

1

1

1

COMEÇAR A UTILIZAÇÃO

A

Coloque a bracelete.

B

Prima “Utilizador 1/Utilizador 2” para ativar o monitor. Este completará o

procedimento de medição automaticamente.

2~3cm

30

1

REGISTOS

Prima o botão para aceder à memória. Prima o botão Utilizador 1 ou Utilizador 2
para avançar ou retroceder nos registos.

PT

Prima o botão
o botão durante 3 segundos para eliminar Registos. O LCD apresenta a informação

“dEL ALL” , prima novamente o botão

No Modo de Chamada de Memória, prima e mantenha premido

para conrmar

SUGESTÕES DE MEDIÇÃO

Ótimo Normal

SYS <120 120-129 130-139 140-159 160-179 ≥180

DIA <80 80-84 85-89 90-99 100-109 ≥110

Elevada-

normal

Ligeira Moderato Grave

RESOLUÇÃO DE PROBLEMAS

E1 Erro de comunicação. Verique o aplicativo e Bluetooth
E3 O manguito não é seguro. Refasten o manguito.
E10/11 O monitor detetou movimento durante a medição.
E20 O processo de medição não deteta batimentos cardíacos.
E21 Medição incorreta.
Eexx Ocorreu um erro de calibração.
Lo Bateria fraca. Carregue a bateria.

GARANTIA & PROTEÇÃO AMBIENTAL

Este aparelho é garantido 2 anos contra qualquer defeito material e de fabrico.
Durante este período, os defeitos serão reparados gratuitamente (uma prova de
compra deve ser apresentada se a balança estiver abrangida pela garantia).
Esta garantia não cobre os danos resultando de acidentes, utilização incorrecta
ou negligência. Se quiser apresentar uma reclamação, dirija-se em primeira
instância à loja onde comprou o aparelho.

Equipamentos elétricos desativados não devem ser eliminados juntamente com
os resíduos domésticos. Entregue num ponto de reciclagem existente. Consulte as
autoridades locais ou o revendedor para obter informação sobre a reciclagem.

31

General Description

* Thank you for selecting TERRAILLON Blood pressure Monitor (LS808-B).

The monitor features blood pressure measurement, pulse rate measurement
and the result storage. The design provides you with two years of lifetime.

* This manual contains important safety information and caution, and provides

step by step instructions for using the product.

* Please do read this user manual carefully and thoroughly before use.

FEATURES:

86.1mm×24mm Blue LCD Display with White Backlight

Measure-during-inating Technology

Up to 60 pieces of record stored

Indications for Use

The TERRAILLON Blood Pressure Monitor is digital monitors intended for use in measuring
blood pressure and heartbeat rate with arm circumference ranging from 22 cm

to 32 cm ( about 8¾˝-12½˝ ).

It is intended for adult indoor use only.

Measurement Principle

This product uses the Oscillometric Measuring Method to detect blood pressure.

Before every measurement, the unit establishes a “zero point” equivalent to the
atmospheric pressure. Then it starts inating the cuff.

Meanwhile, the unit detects pressure oscillation generated by beat-to-beat
pulsatile, which is used to deter-mine the systolic pressure and diastolic pressure
as well as pulse rate.

The device also compares the longest and the shortest intervals of detected
pulse wave to with the average value, and then calculates the standard
deviation.

32

Safety Information

The below signs might be in the user manual, labeling or other components.
They are the requirement of standard and using.

Symbol for “THE OPERATION GUIDE
MUST BE READ”

Symbol for “COMPLIES WITH
MDD93/42/EEC REQUIREMENTS”

Symbol for “TYPE BF APPLIED PARTS”

Symbol for “ENVIRONMENT PROTECTION

- Electrical waste products should not
be disposed of with household waste.
Please recycle where facilities exist.

Symbol for “MANUFACTURER”

Check with your local authority

or retailer for recycling advice”

Symbol for “DIRECT CURRENT”

Symbol for “Authorised Representative

Symbol for “SERIAL NUMBER”

The Bluetooth Combination Mark

EC REP

in the European Community”

T1A/250V 3.6*10CCC

Symbol for “MANUFACTURE DATE For indoor use only

Symbol for “Class II Equipment”

Caution: These notes must be
observed to prevent any damage

Symbol for “Including RF transmitter”

to the device.

CAUTION

This device is intended for adult use only. This device is intended for no-invasive measuring and monitoring of arterial blood
pressure. It is not intended for use on extremities other than the arm or for functions other than obtaining a blood pressure
measurement. Do not confuse self-monitoring with self-diagnosis. This unit allows you to monitor your blood pressure. Do
not begin or end medical treatment without asking a physician for treatment advice. If you are taking medication,consult
your physician to determine the most appropriate time to measure your blood pressure. Never change a prescribed
medication without consulting your Physician. When the device was used to measure patients who have common

arrhythmias such as atrial or ventricular premature beats or atrial brillation, the best result may occur with deviation.

Please consult your physician about the result. If the cuff pressure exceeds 40 kPa (300 mmHg), the unit will automatically

deate. Should the cuff not deate when pressures exceeds 40 kPa (300 mmHg), detach the cuff from the arm and
press the corresponding user button to stop ination. The equipment is not AP/APG equipment and not suitable for use
in the presence of a ammable anesthetic mixture with air of with oxygen or nitrous oxide. The operator shall not touch

output of adapter and the patient simultaneously. To avoid measurement errors, please avoid the condition of strong

electromagnetic eld radiated interference signal or electrical fast transient/burst signal. The user must check that the

equipment functions safely and see that it is in proper working condition before being used. This device is contraindicated
for any female who may be suspected of, or is pregnant. Besides providing inaccurate readings, the effects of this device
on the fetus are unknown. Manufacturer will make available on request circuit diagrams, component parts list etc. This unit is

not suitable for continuous monitoring during medical emergencies or operations. Otherwise, the patient’s arm and ngers

will become anaesthetic, swollen and even purple due to a lack of blood. Please use the device under the environment
which was provided in the user manual. Otherwise, the performance and lifetime of the device will be impacted and
reduced. During use, the patient will be in contact with the cuff. The materials of the cuff have been tested and found to
comply with requirements of ISO 10993-5:2009 and ISO 10993-10:2010. It will not cause any potential sensization or irritation

reaction. Please use ACCESSORIES and detachable partes specied/ authorised by MANUFACTURE. Otherwise, it may

cause damage to the unit or danger to the user/patients. The device doesn’t need to be calibrated within the two years
of reliable service. Please dispose of ACCESSORIES, detachable parts, and the ME EQUIPMENT according to the local
guidelines. If you have any problems with this device, such as setting up, maintaining or using, please contact the SERVICE
PERSONNEL of TERRAILLON. Don’t open or repair the device by yourself. Please report to TERRAILLON if any unexpected
operation or events occur. Please use the soft cloth to clean the whole unit. Don’t use any abrasive or volatile cleaners.

33

Tips for Measurement

Measurements may be inaccurate if taken in the following circumstances.

Within 1 hour

after dinner or drinking

Within 20 minutes

after taking a bath

In a very cold

environment

Immediate measurement

after tea, coffe, smoking

When talking or moving

your ngers

When you want

to discharge urine

34

Maintenance

To obtain the best performance, please follow below instructions.

Put in a dry place

and avoid the sunshine

Avoid intense shaking

and collisions

Use the slightly damp cloth

to remove the dirt

Avoid immersing it in the water.
Celan it with a dry cloth in case

Avoid dusty environment

and unstable temperature

surrounding

Avoid washing the cuff

35

What are systolic pressure and diastolic pressure?

When ventricles contract and pump blood
out of the heart, the blood pressure reaches
its maximum value in the cycle, which is
called systolic pressure. When the ventricles
relax, the blood pressure reaches its minimum
value in the cycle, which is called diastolic
pressure.

What is the standard blood pressure classication?

The blood pressure
classication published
by World Health Organization
(WHO) and International
Society of Hypertension
(ISH) in 1999 is as follows:

CAUTION

Only a physician can tell your normal BP
range. Please contact a physician if your
measuring result falls out of the range.
Please note that only a physician can tell
whether your blood pressure value has
reached a dangerous point.

Grade 3 hypertension (severe)

110

Grade 2 hypertension (moderate)

100

Grade 1 hypertension (mild)

95

Subgroup: borderline

90

High-normal Blood
Pressure

85

Normal Blood
Pressure

80

Optimal

Blood

Diastolic blood pressure (mmHg)

Pressure

Systolic

blood discharging

press

120 150130 160140 180

Systolic blood pressure (mmHg)

artery

Diastolic

blood entering
vein

relax

Level
Blood
Pressure (mm Hg)

Óptima Normal Normal-alta Leve Moderada Grave

SYS <120 120-129 130-139 140-159 160-179 ≥180

DIA <80 80-84 85-89 90-99 100-109 ≥110

Irregular Heartbeat Detector

An irregular heartbeat is detected when a heartbeat rhythm varies while the unit is
measuring the systolic and diastolic blood pressure.During each measurement, this
equipment records the heartbeat intervals and works out the standard deviation.
If the calculated value is larger than or equal to 15,the irregular heartbeat symbol
appears on the symbol when the measurement results are displayed.

CAUTION

The appearance of the IHB icon indicates that a pulse irregularity consistent with an irregular heartbeat was
detected during measurement. Usually this is NOT a cause for concern. However, if the symbol appears often, we
recommend you seek medical advice. Please note that the device does not replace a cardiac examination, but
serves to detect pulse irregularities at an early stage.

36

Why does my blood pressure

uctuate throughout the day?

1. Individual blood pressure varies
multiple times everyday. It is also
affected by the way you tie your cuff
and your measurement position, so
please take the measurement under
the same conditions.

2. If the person takes medicine, the

pressure will vary more.

3. Wait at least 3 minutes for another

measurement.

Why do I get a different blood
pressure at home compared
to the hospital?

The blood pressure is different even
throughout the day due to weather,
emotion, exercise etc, Also, there is

the “white coat” effect, which means

blood pressure usually increases in
clinical settings.

Is the result the same if measuring
on the right arm?

It is ok for both arms, but there will
be some different results for different
people. We suggest you measure the
same arm every time.

What you need to pay attention
to when you measure your blood
pressure at home:

If the cuff is tied properly.
If the cuff is too tight or too loose.
If the cuff is tied on the upper arm.
If you feel anxious.
Taking 2-3 deep breaths before

beginning will be better for
measuring.

Advice: Relax yourself for 4-5
minutes until you calm down.

37

SPECIFICATIONS

Power supply

Display mode

Measurement mode Oscillographic testing mode

Measurement range

Accuracy

Normal working condition

Storage & transportation condition

Measurement perimeter
of the upper arm

Net Weight Approx.284 g
External dimensions Approx.130.9mm×73mm×29.4mm
Attachment AC Adaptor,user manual
Mode of operation Continuous operation
Degree of protection Type BF applied part

Protection against
ingress of water

Software version V01

Device classication Battery Powered Mode:

3.7V 1000mAH Built-in rechargeable li-polymer
battery, 6V

Blue LCD with White Backlight
V.A.= 86.1mm(L) x24mm(W)

Rated cuff pressure:
0kPa-40kPa(0mmHg-300mmHg)
Measurement pressure: 5.3kPa-30.7kPa
(40mmHg-230mmHg)
pulse value:(40-199)beat/minute

Pressure:
5°C-40°C within±0.4kPa(3mmHg)
pulse value:±5%

Temperature:5°C to 40°C

Relative humidity: ≤85%RH

Atmospheric pressure: 86kPa to 106kPa
Temperature:-20°C to 60°C

Relative humidity: 10%RH to 93%RH
Atmospheric pressure: 50kPa to 106kPa

About 22cm-32cm

IP22, It means the device could protected
against solid foreign objects of 12.5 mm and
greater, and against vertically falling water
drops when ENCLOSURE tilted up to 15°

Internally Powered ME Equipment
AC Adaptor charged Mode:
Class II ME Equipment

1A AC Adaptor

WARNING: No modication of this equipment is allowed.

38

Complied European Standards List

Risk management

Labeling

User manual

General Requirements
for Safety

Electromagnetic
compatibility

Performance
requirements

Clinical investigation

Usability

Software life-cycle processes IEC/EN 62304:2006+AC: 2008 Medical device software

ISO/EN 14971:2012 Medical devices — Application of
risk management to medical devices

ISO/EN 15223-1:2012 Medical devices. Symbols to
be used with medical device labels, labelling and
information to be supplied. General requirements

EN 1041: 2008 Medical equipment manufacturers
to provide information

EN 60601-1: 2006+A1:2013 Medical electrical equipment

- Part 1: General requirements for basic safety and
essential performance

IEC/EN 60601-1-11: 2010 Medical electrical equipment -­Part 1-11: General requirements for basic safety and

essential performance - Collateral standard:
Requirements for medical electrical
equipment and medical electrical systems

used in the home healthcare environment
IEC/EN 80601-2-30:2009 Medical electrical equipment ­Part 2-30: Particular requirements for the basic safety

and essential performance of automated

noninvasive sphygmomanometers
IEC/EN 60601-1-2:2007 Medical electrical equipment -

Part 1-2: General requirements for basic safety

and essential performance - Collateral
standard:Electromagnetic compatibility ­Requirements and tests

EN 1060-1:1995+A2:2009 Non-invasive blood pressure
Part 1: General requirements
EN 1060-3:1997+A2:2009 Non-invasive blood pressure
Part 3: Supplementary requirements for
electromechanical blood pressure measuring system

EN 1060-4: 2004 Automatic Blood Pressure Monitor
overall system Interventional accuracy of the testing
process

IEC/EN 60601-1-6: 2010 Medical electrical equipment -­Part 1-6: General requirements for basic safety and

essential performance - Collateral Standard:

Usability
IEC/EN 62366: 2007 Medical devices - Application of
usability engineering to medical devices

- Software life cycle processes

39

EMC Guidance

1) This equipment needs to be installed and put into service in accordance with
the information provided in the user manual;

2) Wireless communications equipment such as wireless home network devices,
mobile phones, cordless telephones and their base stations, walkie-talkies can
affect this equipment and should be kept at least a distance d=3,3m away
from the equipment.

(Note: As indicated in Table 6 of IEC 60601-1-2:2007 for ME EQUIPMENT, a typical

cell phone with a maximum output power of 2 W yields d=3, 3m at an IMMUNITY
LEVEL of 3V/m)

Athorized Component

1. Please use the TERRAILLON authorized adaptor

Adaptor
Input: 100-240V~50/60Hz 0.3A Max
Output: 6V

1A

CAUTION

1. The battery of LS808-B is built-in rechargeable li-polymer battery, please do not disassemble it by the unauthorized
maintenance personel.

2. Under the normal using, it can charge power about 300 times, if the battery cannot charge the power normally
or the blood pressure monitor cannot use normally, please connect with the authorized maintenance personel.
If measured three times per day, and the battery is fully charged, it can be used for about 20 days.

3. Storge and use the blood pressure monitor at the cool, dry and ventilated environment. Avoid to approach to

the re and the heat source, or it will cause the battery explode.

4. Only can use the TERRAILLON’s authorized AC Adaptor(6V 1A) to charge the power. You cannot use the blood
pressure monitor during the process of charging.

5. During the process of charging, the blood pressure monitor display

When the charging is nished, please pull the plug in time.

6. When charging, shall not touch charging connector and the patient simultaneously.

40

Table 2

Guidance and manufacturer’s declaration – electromagnetic immunity – for all
ME EQUIPMENT and ME SYSTEMS

Guidance and manufacture’s declaration – electromagnetic immunity

The LS802-B is intended for use in the electromagnetic environment specied below.

The customer of the user of the LS802-B should assure that it is used in such an environment

Immunity test

Electrostatic
discharge (ESD)
IEC 61000-4-2

Electrical fast
transient/burst
IEC 61000-4-4

Surge IEC
61000-4-5

Voltage dips, short
interruptions and
voltage variations
on power supply
input lines IEC
61000-4-11

Power frequency
(50Hz) magnetic

eld

IEC 61000-4-8

NOTE UT is the a.c. mains voltage prior to application of the test level.

IEC 60601
test level

±6 kV contact
±8 kV air

±2 kV for power
supply lines

±1 kV line(s)
to line(s)

<5% UT
(>95% dip in UT )
for 0.5 cycle

40% UT
(60% dip in UT )
for 5 cycles

70% UT
(30% dip in UT )
for 25 cycles

<5% UT
(>95% dip in UT )
for 5 sec

3A/m 3A/m

Compliance level

±6 kV contact
±8 kV air

±2kV for
power supply lines

±1 kV
differential mode

<5% UT
(>95% dip in UT )
for 0.5 cycle

40% UT
(60% dip in UT )
for 5 cycles

70% UT
(30% dip in UT )
for 25 cycles

<5% UT
(>95% dip in UT )
for 5 sec

Electromagnetic
environment - guidance

Floors should be wood,
concrete or ceramic tile.

If oors are covered with

synthetic material,
the relative humidity should
be at least 30%.

Mains power quality
should be that of a typical
commercial or hospital
environment.

Mains power quality
should be that of a typical
commercial or hospital
environment.

Mains power quality
should be that of a typical
commercial or hospital
environment. If the user of
LS802-B requires continued
operation during power
mains interruptions, it is
recommended that LS-802-B
be powered from an
interruptible power supply
or a battery.

Power frequency magnetic

elds should be at levels

characteristic of a typical
location in a typical
commercial or hospital
environment.

41

Table 4

Guidance and manufacturer’s declaration – electromagnetic immunity – for
ME EQUIPMENT and ME SYSTEMS that are not LIFE-SUPPORTING

Guidance and manufacture’s declaration – electromagnetic immunity

The LS802-B is intended for use in the electromagnetic environment speci ed below.

The customer of the user of the LS802-B should assure that it is used in such an environment.

Immunity test

Conducted RF
IEC 61000-4-6

Radiated RF
IEC 61000-4-3

IEC 60601
test level

3 Vrms
150 kHz to
80 MHz 3 Vrms

3 V/m
80 MHz to

2.5 GHz

Compliance
level

3 Vrms

Electromagnetic
environment - guidance

Portable and mobile RF
communications equipment should
be used no closer to any part of the
LS802-B, including cables, than the
recommended separation distance
calculated from the equation
applicable to the frequency of the
transmitter.

Recommended separation distance

d = 1.167
d = 1.167 80 MHz to 800 MHz
d = 2.333

800 MHz to 2.5 GHz

where P is the maximum output
power rating of the transmitter
in watts (W) according to the
transmitter manufacture and d is the
recommended separation distance
in metres (m).

Field strengths from  xed RF

transmitters, as determined by an
electromagnetic site survey,
be less than the compliance level in
each frequency range.

a

should

b

Interference may occur in the vicinity
of equipment marked with the
following symbol:

NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation

is affected by absorption and re ection from structures, objects and people

a

Field strengths from  xed transmitters, such as base stations for radio (cellular / cordless) telephones and land mobile

radios, amateur radio, AM and FM radio broadcast cannot be predicted theoretically with accuracy. To assess the

electromagnetic environment due to  xed RF transmitters, an electromagnetic site survey should be considered. If
the measured  eld strength in the location in which the LS802-B is used exceeds the applicable RF compliance level

above, the LS802-B should be observed to verify normal operation. If abnormal performance is observed, additional
measures may be necessary, such as re-orienting or relocating the LS802-B.

b

Over the frequency range 150 kHz to 80 MHz,  eld strengths should be less than 3V/m.

42

Table 6

Recommended separation distances between portable and mobile RF
communications equipment and the EQUIPMENT or SYSTEM – for ME EQUIPMENT
or ME SYSTEM that are not LIFE-SUPPORTING

between portable and mobile RF communications equipment at the LS802-B.

The LS802-B is intended for use in an electromagnetic environment in which radiated RF
disturbances are controlled. The customer or the user of the LS802-B can help prevent
electromagnetic interference by maintaining a minimum distance between portable and
mobile RF communications equipment (transmittters) and the LS802-B as recommended
below, according to the maximum output power of the communications equipment.

Rated maximum
output power of
transmitter (W)

0.01 0.167 0.167 0.233

0.1 0.369 0.369 0.738
1 1.167 1.167 2.333
10 3.690 3.690 7.338
100 11.67 11.67 23.33
For transmitters rated at a maximum output power not listed above, the recommended

separation distance d in metres (m) can be determined using the equation applicable
to the frequency of the transmitter, where P is the maximum output power rating of the
transmitter in watts (W) according to the transmitter manufacturer.

NOTE 1 At 80MHz and 800MHz, the separation distance for the higher frequency range

applies.

NOTE 4 These guidelines may not apply in all situations. Electromagnetic propagation

is affected by absorption and re ection from structures, objects and people.

Recommended separation distances

Separation distance according to frequency of transmitter (m)
150 kHz to 80 MHz
d = 1.167

80 MHz to 800 MHz
d = 1.167

800 MHz to 2.5 GHz
d = 2.333

EC REP

GUANGDONG TRANSTEK MEDICAL ELECTRONICS CO.,LTD
Zone A, 5/F., Investment Building, No. 12, Huizhan East Rd., Torch
Development District, Zhongshan, Guangdong, 528437, China

MDSS - Medical Device Safety Service GmbH
Schiffgraben 41, 30175 Hannover, Germany

43

Terraillon SAS France & Headquarters

1, rue Ernest Gouin

78290 Croissy-sur-Seine - France

Service Consommateurs : 0 826 88 1789

[e-mail]

Service Après Vente

SAV TERRAILLON chez GEFCO

ZA La Porte des Champs

Bâtiment A

95470 SURVILLIERS

Terraillon UK Ltd

2 The Waterhouse

Waterhouse Street - Hemel Hempstead

Herts HP1 1ES - UK

Tel: [phone] - [e-mail]

Terraillon Asia Pacic Ltd

4/F, Eastern Centre

1065 King’s Road

Quarry Bay - Hong Kong

Tel: + 852 (0)2960 7200

[e-mail]

Terraillon Corp USA

[e-mail]

www.terraillon.com