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• The device must be disposed of in accordance with the EU Directive
2012/19 / EU WEEE (Waste Electrical and Electronic Equipment) for waste
electrical and electronic equipment. If you have any questions, please
contact the local utility responsible for waste disposal.
14 REFERENCE TO STANDARD
Device standard: device corresponds to the requirements of the European
standard for:
• Standard ( for arm BPM with adapter ).
• IEC60601–1–6:2010+A1:2013/EN60601–1–6:2010+A1:2015.
• IEC60601–1:2005+A1:2012/EN60601–1:2006+A11:2011+A1:2013+A12:2014.
• IEC60601–1–2:2014/ EN60601–1–2:2015.
• IEC/EN60601–1–11:2015.
• IEC80601–2–30:2009+A1:2013/EN80601–2–30:2010+A1:2015.
The stipulations of the EU–Guidelines 93/42/EEC for Medical Products Class IIa have
been fulfilled.
15 REMARK
Symbols Meaning
The product complies with Directive 93/42 / EEC concerning medical
products.
Some electrical and electrical equipments forbid to abandon and
disposal at will.
Type B equipment.
The degree of protection against insertion.
The first figure (protection against insertion of foreign solid objects):
2 – protection against insertion of solid objects, the size of more
than 12 mm; fingers or other objects with a length of not more than
80 mm, or solid objects.
The second figure (protection against foreign liquids): 2 – protection
against falling drops, falling objects from above at an angle to the
vertical no more than 15° (the device in the normal position).
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