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Omron M7 Intelli IT - Page 61

Omron M7 Intelli IT
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11. Guidance and Manufacturer’s Declaration
EN60
EN
DISPOSAL
At the end of the life of the product, it must be disposed in
accordance with
national and regional regulations. In medical
establishments, in accordance with the requirements of
SanPin 2.1.3684-21Sanitary and epidemiological requirements for
the maintenance of the territories of urban and rural settlements,
water bodies, potable water and potable water supply, air, soils,
residential quarters, operation of industrial, public premises,
organization and implementation of sanitary and anti-epidemic
(preventive) measures”, the product should be recycled as a Class
A product in accordance with the requirements of the Sanitary
Rules applicable to municipal solid waste management.
Battery Disposal
For battery disposal, please contact special localized collection
points located in your city, or local authorities for detailed information
on where and how to return the batteries for environmentally safe
recycling.
2895901-4A_HEM-7361T-ALRU_IM.fm Page 60 Wednesday, October 26, 2022 10:46 AM
VERIFICATION
The doc
ument for verification is P 1323565.2.001-2018.
Reverification interval 2 years.
The type approval mark is labelled on the accompanying documents.
In accordance with Article 13(4) of Federal Law No. 102-ФЗ [102-FZ]
“On ensuring the uniformity of measurements”, the results of the
calibration are confirmed through the inclusion of information on the
calibration results in the Federal Information Fund for Ensuring the
Uniformity of Measurements. Confirmation of the calibration referring
to the name, model and serial number of the device can also be
found on this website: www.csmedica.ru.

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