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13
This product conforms to the provisions of the EC directive 93/42/EEC (Medical Device
Directive). This device conforms to the following standards:
• EN 60601-1: 2006 + AC:2010: - General requirements for basic safety and essential
performance
• EN 60601-1-2:2007 - Electromagnetic compatibility requirements and tests
• EN 60601-1-11:2010 - Requirements for medical electrical equipment and medical
electrical systems used in the home healthcare environment
• EN 1060-1:1995 + A2:2009 – Non-invasive sphygmomanometers - general
requirements
• EN 1060-3:1997 + A2:2009 - Non-invasive sphygmomanometers - Supplementary
requirements for electro-mechanical blood pressure measuring systems.
• EN 1060-4:2004 - Non-invasive sphygmomanometers - Test procedures to determine
the overall system accuracy of automated non-invasive sphygmomanometers.
MEDICAL ELECTRICAL EQUIPMENT needs special precautions regarding EMC.
For detailed description of EMC requirements please contact an authorized local Service Centre (see
package insert).
Portable and mobile RF communications equipment can aect medical electrical equipment.
Please do not dispose of the product in the household waste at the end of its useful life.
Disposal can take place at your local retailer or at appropriate collection points provided
in your country.
Guarantee
See warranty statement inside the Guarantee/Consumer Card/Authorized Service Centers booklet.
If for any reason you have to return your device to the point of sales or authorized Service Center,
please fully complete the Consumer Card (provided with the device) and insert it inside of the box
before you return your device.
The Consumer Card can also be found in Kaz Europe website (www.hot-europe.com/customer-care/
repair-services/) and you can download it in the case that you lose the one provided with the device.
The LOT and SN of your device are printed on the rating label in the back of the product.
UK only:
This guarantee in no way aects your rights under statutory law.
0297
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