Iec 60601-1:2005/en 60601-1:2006/ac:2010 (Medical electrical equipment --
part 1: General requirements for basic safety and essential performance).
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.
SpecIFIcatIonS
1. product name: tenS device
2. Model: ad-2026
3. number of treatment program: 9
4. range of pulse frequency: 2-80hz
5. range of output voltage: 30V±20% (500)
6. classification: Internally powered, type BF applied part, IpX0,
or apG,continuous operation
7. Machine size: approx.128mm × 56mm × 16mm
8. Weight: approx.67.4g (exclude batteries)
9. power source: batteries: 2 ×1.5V
10. environmental temperature for operation: 5°c~40°c
11. environmental humidity for operation: ≤80%
12. environmental temperature for storage and transport: -20°c~55°c
13. environmental humidity for storage and transport: ≤95%
14. environmental pressure: 80Kpa~105Kpa
15. Battery life: approx.2 months with alkaline batteries and 30-min. usage
per day.
Note: these specifications are subject to change without notice.
notIce
1. If you feel uncomfortable or abnormal of skin, please stop using.
consult with doctors and follow doctor's advice.
2. please don't use it in the bathroom or other place with high humidity.
3. please don't use it when driving or sleeping.
4. do not make any sharp kinks in the connecting leads or electrodes.
5. please don't use it for other purposes except treatment.
6. please do not throw battery into fire.
7. do not use the device if you are connected to, or in the vicinity of, high-
frequency surgical or industrial equipment. this may cause burn
on the skin under the electrodes, as well as problems with
stimulator.
ENGLISH
SIze aaa
22
no ap
injuries
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