VISIOMED BewellConnect BW-PFX1 User Manual Download Page 11

BewellConnect - BW-PFX1 - User Manual - 072017v1

BewellConnect - BW-PFX1 - User Manual - 072017v1

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-  Near of shortwave or microwave therapy equipment, since this may affect the output power 

of the stimulator.

- In case of fever.

People must not be treated with this device in case of:

• Extra-urethral incontinence (fistula, ectopic ureter),

• Overflow incontinence due to outflow obstacle,

• Serious retention of urine in the upper urinary tract,

•  Symptoms of bladder infection, urinary or vaginal infections, localized lesions or other 

undiagnosed symptoms,

• Total/subtotal prolapsed uterus/vagina without doctor advice,

Paris. Postpartum pelvic floor muscle training and abdominal rehabilitation: Guidelines X. Deffieux, S. Vieillefoss and al. Doi : 10.1016/j.

jgyn.2015.09.023

• Epilepsy,

• Irregular menstrual bleeding cycles.

DO NOT USE ON THESE INDIVIDUALS 

- Children or infants, because the device has not been evaluated for pediatric use.

-  This device is not designed for use by people (including children) with reduced physical, 

emotional or mental abilities or those lacking experience or knowledge unless used in the 

presence of someone responsible for their security, under supervision or following instructions 

about how to use the device.

DO NOT USE THIS DEVICE DURING THESE ACTIVITIES

- When in the bath or shower; penetrating water can impair function. 

- While sleeping.

-  When driving, operating machinery, or similar actions needing fine motor control; electrical 

stimulation may cause brief involuntary muscle movements.

1.2. CAUTION

- Do not use MyPeriTens probe for more than 30 minutes per session without medical advice. 

-  If tissue irritation should occur, treatment should be temporarily discontinued. If problems 

continue, contact your health care provider. Hypersensitivity can occur in isolated cases.

- Always turn the power off before removing or changing the location.

-  If the stimulator is not functioning properly or you feel discomfort, immediately stop using 

the device.

-  If you have suspected or diagnosed heart disease, you should follow precautions recommended 

by your physician.

-  If you have suspected or diagnosed epilepsy, you should follow precautions recommended 

by your physician.

-  Consult with your physician prior to using the device after a recent surgical procedure, as 

stimulation may disrupt the healing process.

- Use caution if you have a tendency to bleed internally, such as following an injury or fracture.

-  To minimize the risk of infection, wash your hands thoroughly – preferably with anti-bacterial 

soap – before touching the probe.

-  You should stop using the device and consult with your physician if you experience adverse 

reactions from the device.

1.3. GENERAL PRECAUTIONS

- This product should not encourage self-medication or adaptation of your treatment.

-  Use this device only for the use for which it is designed as described in this manual. Do not use 

for any other purpose except for what it is intended for.

-  Inspect the equipment prior to use, if you detect any problem on the device, do not use it and 

contact customer service.

-  Do not use the device if it is damaged. The continuous use of a damaged unit may cause injury, 

or serious danger.

- The long-term effects of electrical stimulation are unknown.

- Follow the maintenance instructions specified in this manual.

-  Before and after use, the part of the electrode in contact with the body and the silicone sleeve 

should be cleaned – please consult chapter 5.

-  Keep unit away from children. The probe is a choking hazard and the USB cable could cause 

strangulation. The unit contains small pieces that may be swallowed. If swallowed immediately 

contact your physician.

-  Use this device only with the silicone sleeve, adaptor and storage case recommended by the 

manufacturer.

- Do not freeze or microwave the device.

- Do not maintain or repair the device while the device is in use.

- Do not modify this device without authorization of the manufacturer.

-  Use this device in an ambient temperature range of 5°C to 40°C / 41°F to 104°F and humidity 

range : 15% to 90%. 

-  Do not expose this device to extreme temperature conditions > 50°C to < -10°C / > 122°F to 

< 14°F. 

-  This device must always be placed in a clean and dry place in its storage box. Do not store this 

device to extreme humidity (below 0% RH or over 93% RH). Failing to do so may affect the 

performance of the stimulator.

-  Do not expose this device to sunlight or water (unless for light cleaning, see section 5). Never 

immerse the device and the storage case in a liquid.

- Do not use this device outdoors.

- Never drop the device.

Summary of Contents for BewellConnect BW-PFX1

Page 1: ...BewellConnect BW PFX1 User Manual 072017v1 BewellConnect BW PFX1 User Manual 072017v1 26 1 1 BW PFX1 MyPeriTens 0197 MANUFACTURED FOR European market March Europ en...

Page 2: ...anja soporte de carga Orange gef hrt Ladest nder LEXIQUE DES SYMBOLES SYMBOLS EXPLANATION 0197 Marquage CE CE marking Attention Caution Voir le manuel d instructions Avis sur l quipement Suivre les in...

Page 3: ...BewellConnect BW PFX1 User Manual 072017v1 4 5 FR MyPeriTens BW PFX1 0197...

Page 4: ...T APPAREIL DANS LES CONDITIONS SUIVANTES Cet appareil peut causer une arythmie cardiaque fatale chez certaines personnes consultez votre m decin avant de l utiliser Pour des raisons d hygi ne ne parta...

Page 5: ...s probl mes persistent contacter son m decin Une hypersensibilit peut se produire dans certains cas teignez toujours l appareil avant de le retirer ou de le changer d endroit Si la sonde ne fonctionne...

Page 6: ...n toujours entreposer l appareil sur son socle de rangement Ne pas ranger d autres objets sur ce socle 2 USAGE PR VU MyPeriTens est un stimulateur musculaire non implant con u pour traiter l incontine...

Page 7: ...informations suivantes peuvent tre mises jour bw PERITENS T l charger l application MyPeriTens sur smartphone ou tablette depuis l App Store ou Google Play S assurer que le syst me d exploitation est...

Page 8: ...Dur e de traitement 1 99 min Param tres de sortie pour les exercices de renforcement musculaire du p rin e Dur e de contraction 1 60 s Dur e de rel chement 1 60 s Dur e de cycle 1 99 Programmes pr d f...

Page 9: ...POSSIBLES SOLUTION Le voyant de l appareil principal se met clignoter en orange puis l appareil s teint automatiquement Batterie d charg e Recharger la batterie Le voyant de l appareil principal se m...

Page 10: ...isturbances in certain susceptible individuals consult your physician before using this device For hygiene reasons do not share this device with others This device is a single user device meaning only...

Page 11: ...sician Consult with your physician prior to using the device after a recent surgical procedure as stimulation may disrupt the healing process Use caution if you have a tendency to bleed internally suc...

Page 12: ...Muscular Electrical Stimulation TENS Transcutaneous Electrical Nerve Stimulation The Bluetooth is used to achieve wireless control and make it convenient to use with the mobile application available o...

Page 13: ...r immerse the device and the storage case in a liquid Do not clean the device in an autoclave or diswasher Do not clean with boiling water corrosive cleaning agent chemicals Do not dry with abrasive m...

Page 14: ...F Humidity 0 9 RH Atmospheric pressure 70 106Kpa Technology Bluetooth 4 0 Smart Ready Battery 3 7 V 250mAh Li ion Frequency 2400 2483 5 MHz Channel bandwidth 2 MHz 20 dB Types of spread spectrum FHSS...

Page 15: ...BewellConnect BW PFX1 User Manual 072017v1 28 29 NL MyPeriTens BW PFX1 0197...

Page 16: ...personen Raadpleeg uw arts voordat u dit apparaat gebruikt Om hygi nische redenen vragen we om dit apparaat niet te delen met anderen Dit apparaat is een apparaat van een gebruiker dat betekent dat s...

Page 17: ...die door uw arts worden aanbevolen te volgen Als u vermoede of gediagnosticeerde epilepsie heeft dient u de voorzorgsmaatregelen die door uw arts worden aanbevolen te volgen Raadpleeg uw arts voordat...

Page 18: ...etkanookdooreenzorgverlenergebruiktwordenomspecifiekebekkenbodemaandoeningen te behandelen met elektrische stimulatie 3 KENMERKEN Dit apparaat gebruikt elektrische stimulatietherapie voornamelijk voor...

Page 19: ...herinneren tijdens de behandeling 4 2 APPLICATIE DOWNLOADEN De volgende informatie kan worden bijgewerkt bw PERITENS Download de MyPeriTens applicatie op uw smartphone of tablet via de App Store of Go...

Page 20: ...voor de elektrische stimulatie van de bekkenbodem Frequentiebereik 2 100Hz Pulsbreedtebereik 50 350 s Maximale uitgangsspanning 80 V bij 500 ohm belasting Uitgang sintensiteitsniveau 0 80 niveaus Beh...

Page 21: ...EN OPLOSSEN FOUT MOGELIJKE OORZAKEN OPLOSSING LED van het hoofdapparaat verandert in oranje knipperen en schakelt vervolgens automatisch uit De batterij is leeg Volledig opladen LED van het hoofdappar...

Page 22: ...ertos individuos consulte a su m dico antes de usar este dispositivo Por razones de higiene no comparta con otros este dispositivo ste es un dispositivo de un solo usuario lo que significa que s lo un...

Page 23: ...s de su m dico Si tiene sospecha o diagn stico de epilepsia debe seguir las recomendaciones de su m dico Consulte a su m dico antes de usar el dispositivo si ha tenido un procedimiento quir rgico reci...

Page 24: ...iliza terapia de estimulaci n el ctrica principalmente para estimulaci n neuromuscular Las caracter sticas se muestran a continuaci n El dispositivo MyPeriTens tiene dos funciones estimulaci n el ctri...

Page 25: ...l connect fr para obtener m s informaci n sobre ejercicios y funciones del dispositivo 5 MANTENIMIENTO Y ALMACENAMIENTO DEL DISPOSITIVO 5 1 LIMPIEZA Despu s de finalizar el tratamiento cierre la aplic...

Page 26: ...ogramas predefinidos 16 programas Par metros de salida para el masaje de vibraci n Nivel de intensidad de salida 1 10 niveles Programas predefinidos 16 programas Ruido de funcionamiento 60dB distancia...

Page 27: ...icadora del dispositivo principal empieza a parpadear en naranja y luego el dispositivo se apaga autom ticamente La bater a est agotada Cargar a tiempo La luz indicadora del dispositivo principal empi...

Page 28: ...lligen Personen t dliche Herzrhythmusst rungen verursachen konsultieren Sie Ihren Arzt bevor Sie dieses Ger t verwenden Aus hygienischen Gr nden benutzen Sie dieses Ger t nicht gemeinsam mit anderen D...

Page 29: ...Verwenden Sie die MyPeriTens Sonde nicht l nger als 30 Minuten pro Sitzung ohne rztlichen Rat einzuholen WennGewebereizungenauftretensollten solltedieBehandlungvor bergehendabgebrochen werden Wenn die...

Page 30: ...en Sie das Hauptger t und die Anwendung richtig und sicher an Stellen Sie die Ausgangsintensit t auf das Komfortniveau ein Falls Sie sich unwohl f hlen passen Sie die Ausgangsintensit t an oder beende...

Page 31: ...n die Steckdose des Adapters und den Adapter in eine Steckdose Beim Aufladen wird die Kontrollleuchte des Aufbewahrungsbeh lters auf orange wechseln und gr n aufleuchten wenn der Akku vollst ndig aufg...

Page 32: ...eisten verwenden Sie bitte das Hauptger t und das Zubeh r vom Hersteller 6 Wenn Sie das Ger t l ngere Zeit nicht benutzen laden Sie es bitte alle 2 3 Monate auf um die Lithium Akku Leistung zu gew hrl...

Page 33: ...Anzahl der Kan le 40 Kanalabstand 2 MHz Kanalfrequenz 0 39 Kanal 2 402 2 480 GHz Verweilzeit wenn FHSS 400 ms Hopping Rate wenn FHSS 1600 Hz Maximale Ausgangsleistung 4 dBm Mitgeliefertes Zubeh r Hau...

Page 34: ...BewellConnect BW PFX1 User Manual 072017v1 67 E M C D ATA...

Page 35: ...Class A Voltage fluctuations flicker emissions IEC 61000 3 3 Complies GUIDANCE AND MANUFACTURE S DECLARATION ELECTROMAGNETIC IMMUNITY The BW PFX1 is intended for use in the electromagnetic environment...

Page 36: ...site survey should be considered If the measured field strength in the location in which the BW PFX1 is used exceeds the applicable RF compliance level above the DEVICE should be observed to verify n...

Page 37: ...BewellConnect BW PFX1 User Manual 072017v1 73 WA R R A N T Y...

Page 38: ...tenez pas satisfaction des r parations de ce produit veuillez contacter le service clientsVisiomed EN Visiomed will repair or replace this product free of charge in the case of defective parts or manu...

Page 39: ...strucciones de empleo Adem s la presente garant a no cubre los da os relacionados con ca das manipulaciones inadecuadas instalaci n incorrecta da os rela cionados con fuegos inundaciones rayos u otro...

Page 40: ...i nderesiduos dom sticos DE Entsorgung von Elektroger ten durch Benutzer in privaten Haushalten in der EU Weitere Informationen dar ber wo Sie alte Elektroger te zum Recyceln abgeben k nnen erhalten S...

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