Zero-Plus 02392 Скачать руководство пользователя страница 23 | Manualshive

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02392_EN_180x140_GM_V1.indd 23

02392_EN_180x140_GM_V1.indd 23

19.11.2019 15:54:19

19.11.2019 15:54:19

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Содержание 02392

Страница 1: ...02392 EN Operating Instructions from page 3 02392_EN_180x140_GM_V1 indd 1 02392_EN_180x140_GM_V1 indd 1 19 11 2019 15 54 13 19 11 2019 15 54 13...

Страница 2: ...02392_EN_180x140_GM_V1 indd 2 02392_EN_180x140_GM_V1 indd 2 19 11 2019 15 54 16 19 11 2019 15 54 16...

Страница 3: ...sposal______________________________ 19 Safety and Performance Standards ________ 19 Dear Customer We are delighted that you have chosen this ultrasound pain therapy device Before using this device fo...

Страница 4: ...operating instructions before use Energy e ciency class VI Type BF applied part Date of manufacture Manufacturer Supplementary information Specification of the serial number Protection class II devic...

Страница 5: ...pection or maintenance measures The device is not equipped with any parts that need to be maintained by the user The device is protected against unauthorised use Never modify the device without the ma...

Страница 6: ...ases or circulation problems people with incomplete skeletal growth people who have undergone an operation for which the treatment is not yet complete people with carcinogenic lesions people with mali...

Страница 7: ...acute injuries and open wounds benign or malignant tumours eyes uterus testicles genital area This device should not be used to alleviate symptomatic local pain unless the cause of the illness is know...

Страница 8: ...itch the device on see the Operation chapter If the device functions correctly the drop of water will move around the surface area of the ultrasound head or it might even disperse Safety Notices This...

Страница 9: ...ious injuries Failure to follow this specification will cause the warranty to become void DANGER Danger of Electric Shock Use the device only in closed rooms Do not use the device in a wet environment...

Страница 10: ...Operating the device in a way other than the one described here or failure to follow the operating steps described here may cause dangerous ultrasound radiation to be released The device must not be o...

Страница 11: ...technical data matches that of the device and the mains adapter Make sure that the connecting cable is not squashed bent or laid over sharp edges and does not come into con tact with hot surfaces Do...

Страница 12: ...ce local swelling and chronic inflammation The intensity of the ultrasound can be adjusted to deliver the e ect you want Before Initial Use Read through the operating instructions carefully to be able...

Страница 13: ...1 x Device Description 1 Ultrasound head 2 Timer indicator light 5 10 15 3 Button Switch device on o set operating time Press 1 x 5 minutes Press 2 x 10 minutes Press 3 x 15 minutes Press 4 x Switch o...

Страница 14: ...area to be treated with soap or alcohol If the skin is too hairy trim or shave the hair to ensure optimum treatment 2 Applying Ultrasonic Gel Apply a generous amount of ultrasonic gel to the area of...

Страница 15: ...d move it slowly and in a circular motion over the surface of the skin Make sure that you cover the full treatment area evenly Please Note Switch o the device during breaks The circular movement shoul...

Страница 16: ...ou can apply a little detergent if necessary Clean the contact surface immediately after every treatment and make sure that no residues of ultrasonic gel remain on the ultrasound head Disinfect it fro...

Страница 17: ...ice and wait until it has cooled down The device can only be used again once the temperature has fallen below 40 C The device is defective Contact the customer service department or a specialist deale...

Страница 18: ...e range Operation 0 40 C Storage and transport 20 55 C Humidity Operation 30 85 Storage and transport 20 90 Air pressure Operation 70 106 KPa Storage and transport 70 106 KPa Product classification No...

Страница 19: ...ments of the following regulations This device satisfies the requirements of the Medical Devices Directive 93 42 EEC in relation to medical devices Notices on EMC Warning Use of this device in the vic...

Страница 20: ...fore First Use chapter as a result of electromagnetic interference it must not be used and an attempt should be made to use it in a di erent place To maintain the basic safety and performance capacity...

Страница 21: ...180 225 270 and 315 0 UT 1 cycle and 70 UT 25 30 cycles Single phase at 0 0 UT 250 300 cycle 0 UT 0 5 cycle At 0 45 90 135 180 225 270 and 315 0 UT 1 cycle and 70 UT 25 30 cycles Single phase at 0 0...

Страница 22: ...iation 1 kHz sine 2 0 3 28 710 704 787 LTE Band 13 17 Pulse modulation 217 Hz 0 2 0 3 9 745 780 810 800 960 GSM 800 900 TETRA 800 Pulse modulation 217 Hz 2 0 3 28 870 930 1720 1700 1990 GSM 800 900 TE...

Страница 23: ...02392_EN_180x140_GM_V1 indd 23 02392_EN_180x140_GM_V1 indd 23 19 11 2019 15 54 19 19 11 2019 15 54 19...

Страница 24: ...omer service for medical questions 49 0 38851 314337 Mon Fri 8 am midday Technical customer service 49 0 38851 314650 spare parts damage to device http www dspro de kundenservice Calls to German landl...

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