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4. Information on electric and electronic devices collection
locations is available from local government agencies or
from the dealer.
5. Spent or fully discharged single-use and
rechargeable batteries must be discarded in
dedicated labelled bins, turned over to hazardous
waste collectors or returned to electric equipment
dealers.
This product has been designed, manufactured and marketed
in accordance with the requirements of the medical device
directive (MDD) 93/42/EEC, and for that reason the product has
been marked with the CE mark, and a declaration of conformity
has been issued for it, which is made available to market
regulators.
The product complies with the following European standards
applicable to non-invasive blood pressure measuring devices:
EN 1060-1: Non-invasive sphygmomanometers. Part 1: General
requirements.
EN 1060-3: Non-invasive sphygmomanometers. Part 3:
Additional requirements for electro-mechanical blood
measuring systems.
EN 60601-1: Medical electric devices. Part 1: General
requirements for basic safety and essential performance.
EN 60601-1-2: Medical electric devices. Part 1-2: General
requirements for basic safety and essential performance.
Collateral standard: Electromagnetic disturbances —
Requirements and tests.
18. CE DECLARATION
