2.3. W
.
ARRANTY
NOTE.
Upholstery damage caused by contact with clothes or clothing accessories (ex: belts) having metal, sharp, pointed
or similar parts will not be replaced under warranty.
CAUTION.
The use of disinfectants or detergents with a strong alcoholic content on the plastic components of the
equipment may damage the surface of the product, especially the upholstery.
2.4. I
DENTIFICATION AND LABELLING
The identification label is positioned externally on the chair. It indicates the chair model, serial number and other information.
Figure 1 highlights the label position and a facsimile.
FIG. 1
Manufacturer
Model. It identifies unambiguously the device
of the product family
Medical device
Read the operating instruction carefully
CE marking
2.5. T
ECHNICAL SPECIFICATIONS
2.5.1.
Sector-specific standard compliance.
The gynaecological patient chair model SERENITY NEXT complies with the Regulation (EU) 2017/745 (MDR), concerning med-
ical devices.
In particular, design and manufacture of the equipment comply with the following international standards:
▪
EN 60601-1:2006 / A11 A1;
▪
EN 60601-1-2:2015.
.
.
– 34 –
Operating instructions
Manufacturing date
Serial number of the device
UDI code. UDI coding may not be shown on
the label
Contains type B applied parts
Dispose of the product in compliance with
the procedures provided for electric and
electronic equipment