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English
Applied part of type BF.
Disposal in accordance with Directive 2012/19/EU (WEEE).
Complies with the European Medical Device Directive
(93/42/EEC) and amended by directive 2007/47/EC
requirements. Notified body TÜV Rheinland (CE0197).
The name and the address of the manufacturer.
Manufacturer:
Name: Shenzhen Dongdixin Technology Co., Ltd.
Add:
No. 3 Building XiliBaimang Xusheng industrial
Estate 518108, Nanshan Shenzhen, China
Tel: 0086-755-27652316
Fax: 0086-755-27652674
• Ensure that electrode pads and cables are undamaged before use.
• The TENS/EMS machine may only be used in conjunction with
the accompanying accessories.
• Treatment may not be given above the neck, i.e. to the face, on the throat,
or anywhere on the head.
• Stimulation should not take place while the user is connected to high-
frequency surgical equipment, it may cause burn injuries on the skin under
the electrodes, as well as problems with the stimulator.
• Do not use the stimulator in the vicinity of shortwave or microwave therapy
equipment, since this may affect the output power of the stimulator.
• Do not use the device on children, as it has not been evaluated for
pediatric use. Keep the stimulator out of reach of children to avoid
inhalation or swallowing of small parts. The cable may cause strangulation.
• This device is designed for use by and on a single adult person.
• For hygienic reasons electrodes should not be shared.
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