Braun VitalScan 1 Manual Del Usuario página 22

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Continuous Operation
IP22: Protected against solid foreign objects of 12.5 mm diameter and greater.
Protected against vertically falling water drops when the device is tilted up to 15°
This device conforms to the following standards:
EN 60601-1: «Medical electrical equipment» –
Part 1: General requirements for safety
EN 1060-1: AMD 1 «Non-invasive sphygmomanometers» –
Part 1: General requirements
EN 1060-3: «Non-invasive sphygmomanometers» –
Part 3: Supplementary requirements for electro-mechanical blood pressure
measuring systems
EN 1060-4: Non Invasive Sphygmomanometers
Part 4: Test Procedures to Determine the Overall System Accuracy of Automated
Non-Invasive Sphygmomanometers
AND
EN 60601-1-2 Medical Electrical Equipment-
Part 1-2: General Requirements for Basic Safety and Essential Performance- Collateral
Standard: Electromagnetic Compatibility-Requirements and Tests
AND
EN 60601-1-11: Medical Electrical Equipment
Part 1-11: General Requirements for Basic Safety and Essential Performance-
Collateral Standard: Requirements for Medical Electrical Equipment and Medical
Electrical Systems Used in the Home Healthcare Environment
This product conforms to the provisions of the
EC directive 93 /42 / EEC (Medical Device Directive).
0297
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.
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