Braun ExactFit 3 Manual page 11

IMPORTANT
Read the operating instructions.
Classification:
• Internally powered equipment
• Type BF equipment
• IPX0
• Not suitable for use in the presence of flammable anesthetic mixture with air,
oxygen or nitrous oxide
• Continuous operation with short-time loading
Operating temperature
Storage temperature
This device conforms to the following standards:
• EN 60601-1: 1990 + A1: 1993 + A2: 1995 + A13: 1996 General requirements for safety.
• EN 60601-1-2: 2001 - Electromagnetic compatibility requirements and tests.
• EN1060-1: 1995 + A1: 2002 - Non-invasive sphygmomanometers- General
requirements .
• EN1060-3: 1997 + A1: 2005 - Non-invasive sphygmomanometers- supplementary
requirements for electromechanical blood pressure measuring systems.
• EN1060-4: 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 affect 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 that comes with the product.
Keep dry.
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